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Dr Reddys Laboratories Ltd.

BSE: 500124 | NSE: DRREDDY |

Represents Equity.Intra - day transactions are permissible and normal trading is done in this category
Series: EQ | ISIN: INE089A01023 | SECTOR: Pharmaceuticals

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Company History - Dr Reddys Laboratories
 - The Company was Incorporated on 2nd November.  The Company was
 promoted by Dr. K. Anji Reddy and his associates who were also the
 promoters of Standard Organics, Ltd.
 - In May, the Company issued 7,50,000 equity shares of Rs 10 each for
 cash at par linked to 1,50,000 - 15% secured redeemable
 non-convertible debentures of Rs 100 each for cash at par in the
 proportion of one debenture for five equity shares held including the
 oversubscription from the public.  The allotment was made as follows:
 - (i) 12,550 equity shares linked to 2,510 debentures were issued to
 business associates
 - (ii) 850 shares linked to 170 debentures were issued to the
 - (iii) 2,80,500 shares linked to 56,100 debentures issued to the
 non-resident Indians and (iv) 5,25,850 shares linked to 1,05,170
 debentures were issued to the public.
 - 10,06,500 equity shares then issued at par out of which 2,56,500
 equity shares were reserved and allotted to promoters, etc.  The
 remaining 7,50,000 equity shares were issued linked to debentures of
 which the following shares were reserved for preferential allotment:
 - (i) 15,000 shares to business associates of the Company (only
 12,550 shares taken up);
 - (ii) 37,500 shares to employees of the company (only 850 shares
 taken up) and 3,00,000 shares to non-resident Indians (only 2,80,500
 shares taken up).  The balance 3,97,500 shares along with the
 unsubscribed portion of 58,600 shares out of the preferential quota
 were offered for public subscription during June.
 - 1,16,250 additional shares linked to debentures were allotted to
 retain oversubscription (46,500 shares to promoters and 69,750 shares
 to the public.
 - 13,660,500 No of equity shares forfeited.
 - (15 months), a plan was drawn for the expansion and modernisation
 of formulations division.  ICICI and IFCI sanctioned term loans of Rs
 198 lakhs and Rs 132 lakhs respectively.
 - An explosion at the Company's plant resulted in stoppage of
 production for 2 months.  Two new products namely, a Ciprolet and
 Enam were introduced by the Company's formulation division while the
 Company's bulk drug division commenced manufacture of ciprofloxacin,
 new drug.  The Company exported goods such as Methyldopa, Cephalexin
 etc., worth Rs 2.68 crores.
 - 6,83,125 rights shares issued (prem. Rs. 15 per share; prop.  1:2).
 Additional 1,02,470 shares allotted to retain oversubscription.
 Another 34,155 shares (prem. Rs 15 per share) allotted to employees.
 - The Company started manufacturing a new bulk drug by the name
 Omeprazole which was launched in the market by the brand name OMEZ. 
 - 10,92,950 bonus equity shares issued in prop. 1:2.
 - 32,78,850 bonus equity shares issued in prop. 1:1.
 - Subject to necessary approvals being obtained, a separate company
 in the name of `Dr. Reddy's Dignostics Ltd.' was to be set up for the
 manufacture of dragnostics kits.  The Company proposes to invert to
 the extent of 60% in the equity capital of the company.
 - The Company proposed to invest Compact Electric Ltd., which was in
 the process of setting up a plant at Chennai for manufacturing energy
 efficient electric filament/discharge lamps in Collaboration with
 Li-Tech Corporation, South Korea.  The Company set up a subsidiary
 `Reddy Hong Kong Ltd.' in Hong Kong for marketing the Company's
 products in Main Land China and Far East countries.
 - `Reddy Biomed Ltd.' was incorporated as a joint venture between the
 Company and a Russian Company `Joint Stock Company of open type named
 after 1:1.  Machnikov' for manufacturing and marketing formulation in
 - Effective 1st April, Standard Equity Fund was merged with the
 Company.  Pursuant to the scheme of amalgamation 2,63,062 equity
 shares of Rs 10 each of the Company were issued to the shareholders
 of erstwhile Standard Equity Fund in the ratio of one equity share of
 Company for ten equity shares of the erstwhile Standard Equity Fund
 - During July the Company issued 4301076 Global Depository Receipts
 at a price of US $11.16 per GDR.  The Company allotted 4301076 equity
 shares of Rs 10 each at a premium of Rs 340 per share underlying the
 - The company issued 4,301,076 GDSs representing 4,301,076 equity
 shares of the Company, par value Rs.10 (Shares), in a private
 placement in 1994 pursuant to Regulation S and Rule 144A under the
 Securities Act of 1933 (the Securities Act). The GDSs are listed on
 the Luxembourg Stock Exchange and each GDS represents one Share. As
 of May 4, 2001, there were 1,789,285 GDSs outstanding representing
 - Formulation division launched two new products namely Lanzap, an
 anti-Ulcerant drug and Peristil, drug for gastric disorder.  The bulk
 drug division commenced the production of six new products viz.,
 Finasteride, Nimesulide, Fluoxetine, Hydrochloride, Terbinafine,
 Hydrochloride, Risperidone and Clozapine.  The Company was in the
 process of setting up a subsidiary in the Antilles Kingdom of
 Netherlands for licensing the manufacture and marketing of drugs.
 - 263,062 equity shares issued to the shareholders of erstwhile
 standard Equity Fund Ltd. Pursuant to the scheme of amalgamation. 
 - Four new products viz. Nise, Stamlo Beta, Sparfloxacin and Finast
 were launched.  Finast, a drug for treatment of benign prostiate
 enlargement was launched for the first time in India.  Under the bulk
 drugs category two new drugs viz. Sparfloxacin & Croratidine were
 - The diagnostics division entered into a technical collaboration
 agreement with Board of Radiation and Isolope, technology for
 manufacture & marketing of radioimmonuassay kits for the production
 of diagnostic and therapeutic recombinant protections, the
 division entered into a technical collaboration agreement with Viral
 Therapeutics Inc. U.S.A.
 - In view of the company's long term plans in the area of diabetic
 care, the company launched Reclide (Glicazide), its first product in
 the theraupeutic segment.  Also, in its commitment to promote
 innovative products, the company entered into a marketing alliance
 market Netacryl, a bio adhesive (n-butyl-2-cyno acrylate) used for
 the closure of external surgical and post traumatic wounds. 
 - The Company set up a Critical care division to commercialise
 products from the research foundation and the first product to be
 marketed by the division was Miitotax an anti-cancer product used in
 the treatment of breast and ovarian cancer.
 - The city-based drug major Dr. Reddy's Laboratories has perfected
 the formulation of an anti-diabetic compound, glitazone for
 commercial marketing.
 - DRF has signed a licensing agreement with the Denmark-based Novo
 Nordisk, according to which the latter would obtain an exclusive
 worldwide license to develop and market pharmaceutical products based
 on compounds discovered and patented by the former.
 - Dr. Reddy's Research Foundation has finally signed the agreement
 for clinical testing of its four diabetes compounds of glitazone with
 the European drug major; Nova Nordisk.
 - Dr Reddy's Labs, the Hyderabad based pharmaceutical company, is
 forming two new joint ventures in Brazil and Uzbekistan. 
 - The Hyderabad-based Dr Reddy's Laboratories is manufacturing an
 anti-ulcer formulation right from the basic stage for competitor,
 Ranbaxy Laboratories, as part of its strategy aimed at creating more
 value for its bulk drugs.
 - Dr. Reddy's Laboratories (DRL) has launched its first anti-cancer
 drug Mitotax (Paclitaxel).  The product is produced in-house at Dr.
 Reddy's Research Foundation (DRF) from the extracts of the yew tree
 and formulated in a dedicated facility in Hyderabad.
 - Dr. Reddy's Laboratories (DRL) has ended its collaboration with the
 French company, bioMerieux.  The collaboration agreement, which
 envisaged DRL to market bioMerieux's diagnostic reagents and
 instruments in India, has come to an end on 13th November.
 - Dr. Parvinder Singh, Chairman & Managing Director of Ranbaxy
 Laboratories and Dr. K Anji Reddy, Chairman of the Rs 5000 million
 Dr. Reddy's Group of pharmaceutical companies, were conferred with
 the prestigious `Ishidate Award' of the Federation of Asian
 Associations (FAPA).
 - The merger with Cheminor Drugs (the swap ratio at nine shares of 
 Dr. Reddy's Laboratories for 25 shares of Cheminor), has made  DRL
 the third largest pharmaceutical company in Inida with  participation
 in every element of the value chain.
 - Dr. Reddy's Laboratories Ltd. (DRL) has set up an in-house effluent
 treatment plant at its bulk pharmaceuticals manufacturing facility
 located at Bollaram Industrial Development Area.
 - Dr. Reddy's Laboratories is setting a new trend in the Indian
 pharmaceutical sector by installing a `satellite' discovery research
 laboratory in the United States.
 - The company has two US-FDA approved plants. It has been exporting
 its products to the UK, Switzerland, Germany, Spain, Italy and the
 Netherlands. It also started exporting its formulations in a big way
 to Russia and has set up an office there. DRL has signed a joint
 venture agreement with the Khetan group, Nepal, for setting up a
 joint venture for the manufacture and marketing of finished
 formulations in Nepal and other neighbouring countries. It also
 signed a marketing and distribution agreement with Organics, Israel,
 for a wide range of
 sophisticated diagnostic kits. The products are recognized by WHO and
 other leading organisations in the healthcare industry.  
 - Dr. Reddy's Laboratories and the Gribbles Group of Australia have
 signed a memorandum of understanding to form a joint venture company
 for establishing a network of 50 pathology laboratories and up to 200
 specimen collection centres in India over the next five years.
 - The Board has approved merger of Cheminor Drugs Ltd. with the
 company.  Nine equity shares of the company will be allotted for
 every 25 equity shares of CDL held.  The Company has decided to issue
 7,50,000 equity shares under ESOS.
 - The employees of the formulation unit-II of the company at
 Bachupally have decided to go on an indefinite strike from 17th
 - The Company has introduced a five-day week from January and change
 in timings.  A small group of employees has called for a strike from
 June  19.
 - For the first time in the country, pharma major Dr. Reddy's
 Laboratories has launched an initiative to document clinical studies
 of drugs on the Internet.
 - DRF 2725, an anti-duabetic molecule discovered by Dr. Reddy's
 Research Foundation and licensed to Novo Nordisk in June 1998, has
 entered phase II trials of clinial development.
 - Dr. Reddy's Laboratories Ltd., the Hyderabad-based pharmaceutical
 company, has acquired three brands in the segment of women's health
 from Dai-Ichi Karkaria Ltd.
 - In a move to enhance the market share in the domestic formulations
 segment, Dr. Reddy's Laboratories Ltd.  has decided to set up a
 specialised field-force to work in close partnership with the medical
 community besides regroupes its older products. 
 - The company has entered into an exclusive co-marketing and
 development agreement with Par Pharmaceuticals Inc. covering fourteen
 generic pharmaceuticals products.
 - In April 2001, as a first step towards taking its molecules through
 clinical development on its own, Dr. Reddy's Laboratories has selected
 Simbec Research Limited, a well-known UK-based Clinical Research
 Organization (CRO), for conducting clinical trials of DRF 4832. DRF
 4832 is a PPAR agonist fo r treatment of cardiovascular
 - Dr. Reddy's Laboratories Ltd. has ended a two-year-old marketing
 partnership with the US-based Schein Pharmaceutical Inc following
 Schein's takeover by Watson Pharmaceutical Inc.
 - The Company has entered into an exclusive co-marketing and
 development agreement with Par Pharmaceuticals Inc., the US-based
 manufacturer and distributor of a broad line of generic drugs.
 - Dr Reddys Laboratories has gone online with all its phase III and
 phase IV clinical trials on new products using an application being
 deployed on a website.
 -Eli Lilly has sued Dr Reddy's for infringement of one of the patents
 on olanzapine, the key ingredient in Lilly's antidepressant drug
 - Reddy US Therapeutics, Inc, a biopharmaceutical company based in
 suburban Atlanta and a subsidiary of Dr Reddys Laboratories Limited,
 has announced the formation of a scientific advisory board consisting
 of scientists and physicians to advise it on its drug discovery
 research and development programes.
 - Dr. Reddy's Laboratories Ltd's product insert of its human
 recombinant granulocyte colony stimulating factor -- Filgrastim
 injection (Grastim), an anti-cancer formulation -- has got approval
 from the Drug Controller Gene ral of India (DGCI).
 - In April 2001, Dr. Reddy's Laboratories began trading on the New
 York Stock Exchange (code: RDY). The price to the public per ADS was
 $10.04. Total amount raised (net) was $ 124 million. 
 - In May 2001, the company decided to terminate the GDS programme.
 Once the facility is terminated, the Shares underlying the GDSs will
 be deposited in Dr. Reddy's American Depositary Share (ADS) facility
 with Morgan Guaranty Trust Company of New York as depositary (the
 In May 2001, Novartis Pharma AG and Dr. Reddy's Laboratories
 announced that they have entered a licensing agreement for a novel
 anti-diabetes agent. Under terms of the agreement Dr. Reddy's will
 grant Novartis worldwide exclusive rights to development and
 commercialisation of their insulin sensitiser DRF 4158 in type 2
 diabetes, in return for up 
 to USD 55 million in upfront and milestone payments for specific
 clinical and regulatory endpoints, as wellas royalties. Dr. Reddy's
 will have co-promotion rights for DRF 4158 in India.
 - The agreement has received US regulatory clearance and has become
 effective from July 30, 2001. This event has triggered an upfront
 payment of 5 million US dollars from Novartis. Dr. Reddy's
 hasreceived this payment.
 - The Board has appointed Mr. Krishna G.Palepu as Additional Director
 on the Board of the Company.
 - Dr Norton Peet to head Dr. Reddy's discovery services venture.
 - Appointment of Mr Anupam Puri as Additional Director, Recommended a
 dividend of Rs 2.50 on equity share of Rs 5 each. To convene AGM on
 August 26, 2002, To re-appoint Mr Satish Reddy as Managing Director
 and COO for a period of 5 years wef October 01, 2002 subject to the
 approval of the shareholders.
 -Dr Reddy's appoints Uday Saxena as Chief Scientific Officer.
 -Dr Reddy's Laboratories Ltd has informed that the Company has
 granted 1813 stock options to an employee of the Company at the
 meeting of the Compensation Committee of Board of Directors held on
 August 26, 2002.The options have been granted at a price of Rs 884
 per option, which is equivalent to weighted average share price of
 the Company of last 30 days on BSE.
 -DataEdge deploys direct material procuremet solution for Dr Reddy's
 -DCGI orders for the removal of word 'filgrastim' from its
 anti-cancer drug Grastim
 -Introduces VRS scheme in the company
 -Decides to revoke interim dividend of Rs 2 per share
 -Signs definitive agreement to acquire BMS Lab & Meridian Healthcare
 -Pondicherry unit starts operations
 -Files application for a new drug- amlodipine maleate
 -Launches Bicalutamide under the brand name 'Tabi' which is indicated
 for the treatment of advanced prostate cancer
 -Launches Montelukast (generic name), a non-steroidal drug indicated
 for prohylaxis and treatment of asthma, in India
 -Unveils asthma drug Emlucast
 -Launches Mizolastine, non-sedative anti-histamine drug under the
 brand name Elina
 -Grants 2,59,400 stock options under ESOP (Employee Stock Option
 -Anti-cancer molecule DRF-1042 completes phase I clinical trials
 -Files an Abbreviated New Drug Application (ANDA) with the US Food &
 Drug Administration (FDA) for Clopidogrel Bisulfate tablets 75 mg
 with Para IV certification on all listed Orange Book patents
 -Hikes annual spend on R&D from 6% to 8% of turnover
 -Leads among Indian companies in getting international patents
 -Files Paragraph IV certifications on two patents for Pfizer's
 -Pfizer files suit against Dr Reddy's over Norvasc patent
 -Announces USFDA approval for Tizanidine HCL tablets
 -Gets USFDA approval for Zanaflex
 -Gets final approval from US Food and Drug Administration (USFDA) for
 its Abbreviated New Drug Application (ANDA) for Ciprofloxacin Tablets
 100, 250, 500 and 750 mg
 -Announces ANDA filing for Terbinafine tablets
 -Novo Nordisk announces its decision to suspend the  ongoing clinical
 trials on the anti-diabetic molecule of Dr Reddy's Laboratories Ltd.
 -Values its brand at Rs 3,362 crore in March 2002
 -Judgment of US court goes against Dr Reddy's Laboratories in a
 patent violation case over the antibiotic Cipro
 -Promoters  holding slips from 31.5% to 26%
 -Gets ex-parte temporary injunction stopping Sun Generics from
 manufacturing and marketing pharmaceutical preparations bearing the
 trademark OMZ 20
 -Launches Dr. Reddy's Foundation For Health Education
 -Launches Breast Cancer Helpline in Mumbai
 -Receives USFDA approval for Amlodipine Maleate
 -Launches Broncho-Vaxom for patients suffering from repeated
 respiratory tract infections
 -Launches OncoQuest, India's first real time helpline for doctors
 -Unveils Omeprazole in injectable form in the domestic market
 -Wins the case against Pfizer in US court
 -Wins national award for excellence in corporate governance
 -Withdraws paediatric dosage of Nimesulide from the market
 -Launches Ibuprofen - First product under Dr Reddy's label in the US
 -Unveils Tolterodine Tartrate drug for the treatment of urinary
 -Novartis discontinues trials on Dr Reddy's compound DRF-4158
 -Drops three new compounds from its research pipeline that were
 undergoing or had completed pre-clinical development or animal
 -Dr Reddy's anti-diabetis drug receives a set back as Danish Pharma
 company Novo Nordisk suspends the trails on the drug
 -Announces completion of Insulin trails by Novo Nordisk
 -Pfizer files patent application against Dr Reddy's
 -Announces the completion of a 15 year agreement with Leiner Health
 -Filed a second case against Pfizer in the US
 -Announces ANDA filing for Olanzapine ODT
 -Aventis sues Dr Reddy's Lab for patent infringement
 -Announces ANDA filing for Ondansetron HC1 Tablets, Equivalent to 16
 mg Base
 -Dr. Reddys Board approves merger of Zenovus Biotech Ltd., a wholly
 owned subsidiary
 -Files a new drug application (NDA) with the US Food and Drugs
 Administration (USFDA)
 -Gets US approval for Serzone generic
 -Dr Reddy's complaint on Sertraline dismissed
 -Closes down its 14 year old diagnostic business
 -DRL's brand value estimated at Rs 2,767 crore, human resources
 valued at Rs 2,908 crore as on 31/03/2003
 -Eli Lilly agrees to dismiss with prejudice its wilful infringement
 claim in Olanzapine patent challenge
 -Announces ANDA filing for Rosiglitazone Maleate
 -Glaxo files suit over Dr Reddy's for patent infringement
 - Gets  USFDA approval for Nefazodone HCL tablets
 -Dr. Venkateswarlu retires from Dr Reddy's Laboratories Board
 -Company has announced that it has signed an agreement with PLIVA for
 development and marketing of oncology products in Europe.
 -Dr Reddy's files Abbreviated New Drug Application with USFDA for
 -Dr Reddy's appoints Dr Dennis Langer as President for North America
 -Rotary Club presents Vocational excellence award to Anji Reddy
 -Launched Redotil (racecadotril), the first anti-hypersecretory agent
 for the management of acute diarrhea in India
 -Dr Reddy's Laboratories shifts North American headquarters from its
 old home office in Upper Saddle River in New Jersey to more modern
 facilities in the Somerset Corporate Centre at Bridgewater in central
 New Jersey
 - Dr Reddy's acquires US firm Trigenesis
 - Dr Reddy's' Omez gets 'WordStar' award
 -Dr Reddy's Laboratories Ltd, the Hyderabad-based global
 pharmaceutical major, has obtained the tentative approval of the
 United States Food and Drugs Administration (USFDA) for the
 abbreviated new drug application filed on Fluconazole, indicated for
 the treatment of fungal infection
 -  Receives approval from US Food and Drug Administration (FDA) for
 ciprofloxacin tablets.
 -Establishes new captive BPO unit
 -Dr. Reddy's wins award for energy management
 -Dr Reddys launches India's first drug for treatment of diabetic foot
 -Dr Reddys wins WorldStar awards for anti-counterfeit & patient
 protection packaging
 -DRL unveils new programme for underprivileged youth
 -India's Dr Reddy's Laboratories Ltd has received approval from the
 US Food and Drug Administration to market nizatidine tablets in
 multiple strengths
 -Dr Reddys sets up India's first major drug development company
 -Dr Reddys launches 'Voboliv' Metaoxine to enter hepatoprotactives
 -Dr Reddys announces the launch of Save The Foot initiative to reduce
 Diabetic Food Amputations
 -Dr Reddys Laboratories Ltd has informed that the Company has entered
 into an agreement with Merck
 -Dr Reddys Laboratories Ltd has launches 'Z&D'- a Zinc Sulphate
 formulation indicated as Adjuvant therapy along with ORS in the
 management of Acute and persistent Diarrhea. Available in 10 & 20 mg
 Dispersible orange flavoured Tablets as well as in 10mg/ml & 20mg/ml
 Dry Syrup for pediatric use, this product is intended to supplement
 the ORS (Oral Rehydration Salt) market.
 -Dr Reddy's launches 'Doxobid' - a new oral bronchodilator for asthma
 -Dr Reddys Laboratories Ltd has filed a shelf registration statement
 on Form F-3 with the U.S. Securities and Exchange Commission relating
 to a proposed offering of American Depositary Shares, or ADSs of up to
 13.5 million shares, excluding the underwriter's over-allotment
 -Dr. Reddy's Laboratories has given the Bonus in the Ratio of 1:1
 - Dr Reddy's Laboratories Ltd rolled out Redituxa, its brand of
 rituximab, a monoclonal antibody (MAb) used in the treatment of
 Non-Hodgkin's Lymphoma (NHL).
 -Dr Reddys Laboratories Ltd has appointed Ms. Kalpana Morparia as an
 Additional Director on the Board of the Company by way of a circular
 resolution dated June 05, 2007.
 -Dr. Reddys launches Reditux  Monoclonal Antibody Treatment for
 Non-Hodgkins Lymphoma
 -Dr. Reddys is the first company to get USP certification for its
 -Dr. Reddy's launches Glimy MP 1 and Glimy MP2. 
 Triple drug combination ideal to address the triple defects in
 - Dr Reddys Laboratories Ltd has acquired Jet Generici Sri, a Company
 engaged in the sale of generic finished dosages in Italy.
 -Dr Reddy's Laboratories Ltd has signed a definitive agreement to
 acquire BASF's pharmaceutical contract manufacturing business and
 related facility in Shreveport, Louisiana, USA.
 - Hyderabad: Dr Reddy's Laboratories Ltd unveiled Omez Insta for
 patients suffering from severe gastritis and those on Ryle's tube
 feeding in India.
 - Dr Reddys Laboratories Ltd has appointed Dr. Bruce L A Carter as an
 Additional Director on the Board of the Company.
 - Dr Reddys Laboratories Ltd has has appointed Dr. Ashok S Ganguly as
 an Additional Director on the Board of Directors of the Company with
 effect from October 23, 2009.
 -Dr. Reddy's launches Strea C10 and Strea A15 in India
 -Dr. Reddy's launches Bispec in India
 -Dr. Reddy's joins American Chemical Society Green Chemistry
 Institute Pharmaceutical Roundtable
 - Dr Reddy's Laboratories announced the launch of Cresp. It is a
 darbepoetin alfa that is approved for the treatment of anemia. It is
 due to chronic kidney disease or chemotherapy.
 -Dr. Reddy's announces the launch of Pantoprazole Sodium
 delayed-released tablets.
 -Dr Reddy's launches Levocetirizine tablets in US
 -Dr Reddy's launches generic allergy drug in US
 -Dr. Reddy's announces completion of the acquisition of US penicillin
 facility and products from GlaxoSmithKline
 -Dr. Reddy's announces the launch of Over-the-Counter Fexofenadine
 HCI tablets.
 -Dr. Reddy's launches pegfilgrastim in India under the brand name
 -Registered Office of the Company has been shifted To 8-2-337, Road
 No. 3, Banjara Hills, Hyderabad - 500034, Andhra Pradesh, India.
 -Dr. Reddy's announces the Launch of Ziprasidone Hydrochloride
 -Dr. Reddy's launches of Quetiapine Fumarate Tablets.
 -Dr. Reddy's announces the launch of Olanzapine tablets.
 -Dr. Reddy's announces the Launch of Clopidogrel Tablets, USP.
 - Dr. Reddys announces the Launch of SILDENAFIL TABLETS.
 -Dr. Reddys declares Offer for OctoPlus unconditional.
 -Dr. Reddys announces the Launch of Desloratadine ODT (Orally
 Disintegrating Tablets).
 -Dr. Reddys announces the Launch of Divalproex Sodium Extended -
 Release Tablets, USP.
 -Dr. Reddys announces the Launch of Donepezil Hydrochloride Tablets,
 23 mg.
 -Dr. Reddys Announces the Launch of Zoledronic Acid Injection.
 -Dr. Reddys announces the approval of Azacitidine for Injection
 -Dr. Reddys announces the Launch Decitabine for Injection.
 -Dr Reddys announces the Launch of Zoledronic Acid Injection.
 -Dr. Reddys announces the Launch of Paricalcitol Capsules.
 -Dr Reddys annouces the Lanch of Sumatriptan Injection USP,
 Autoinjector System.
 -Dr. Reddys announces the Launch of Fenofibrate Capsules, USP 43 mg
 and 130 mg.
 - Dr. Reddys announces the Launch of Duloxetine Delayed-Release
 Capsules USP.
 -Dr. Reddys announces the Launch of Docetaxel Injection USP.
 -Dr Reddys announces the Launch of Moxifloxacin Hydrochloride
 -Dr. Reddys announces the Launch of Eszopiclone Tablets C-IV.
 -Dr. Reddy's announces the Launch of Valganciclovir Tablets, USP.
 -Dr. Reddys Laboratories enters into partnership with Hetero to
 accelerate access to treatment for Hepatitis C in India
 -Dr. Reddy's Laboratories has entered into a definitive agreement to
 acquire select portfolio of the established brands of Belgium-based
 firm UCB in India, Nepal, Sri Lanka and Maldives for Rs 800 crore
 -Dr Reddys Laboratories has launched the drug, Somazina, an innovator
 brand of Citicoline for stroke patients in India
 -Dr Reddy's Laboratories and AstraZeneca Pharma India Limited entered
 into a distribution agreement for saxagliptin and its fixed dose
 combination with metformin, in Type 2 Diabetes.
 -Dr. Reddy launches HAiROOTZ in India - its first OTC hair growth
 -Dr Reddy's Laboratories has completed the acquisition of select
 portfolio of established brands of foreign biopharma firm UCB in
 India, as per the media reports. 
 -Purdue University has signed a Memorandum of Understanding (MoU)
 with Dr Reddy Laboratories Limited (DRL) to strengthen pharmaceutical
 research and development
 -Dr Reddy's Laboratories has entered into strategic collaboration
 with Amgen, leading independent biotechnology companies
 -PanTheryx and Dr. Reddy's Announce an Agreement to Market
 PanTheryx's Proprietary Nutritional Intervention for Pediatric
 Infectious Diarrhea
 -Dr. Reddys Laboratories signs commercialization deal with
 -Dr. Reddys signs MoU with Life Sciences Sector Skill Development
 Council and Vishnu Institute of Pharmaceutical Education and Research
 to Strengthen the Skilled Labour Pool in the Life Science Industry
 -Dr. Reddys Laboratories and XenoPort Enter Into a U.S. Licensing
 Agreement for XP23829
 -Dr. Reddys Laboratories Acquires the Rights to Investigational
 Anticancer Agent E7777 for U.S, Europe and Certain Emerging Markets
 from Eisai.
 -Dr Reddys Labs launched Omeprazole and Sodium bicarbonate capsules
 in the US market.
 -Dr. Reddy's Laboratories announces the launch of Paricalcitol
 Injection in the U.S. Market
 -Dr. Reddy's Laboratories announces new strategic deal with Gland
 Pharma in the U.S. Market
 -Dr. Reddy's Laboratories announces the launch of Melphalan
 Hydrochloride for Injection in the U.S. Market.
 -Dr. Reddys Laboratories announces acquisition of 100% stake in
 Imperial Credit Private Limited, a Non-Banking Finance Company (NBFC)
 - 'Dr. Reddy's Laboratories announces the launch of Progesterone
 Capsules in the U.S. Market.'
 -Dr. Reddy's Laboratories announces the launch of Cefixime for Oral
 Suspension, USP in the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Sevelamer Carbonate
 Tablets in the U.S. Market.
 -Dr. Reddy's expands commercial operations in Europe.
 -Dr. Reddys and Integra LifeSciences enter into an agreement to
 market and distribute DuraGen Plus and Suturable DuraGen Dural
 Regeneration in India
 -Dr. Reddy's Laboratories announces the launch of Ezetimibe and
 Simvastatin Tablets in the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Resof Total in
 -Dr. Reddy's Laboratories announces the launch of Sevelamer Carbonate
 for Oral Suspension in the U.S. Market.
 -Dr. Reddy's Laboratories launches Aspirin and Extended-Release
 Dipyridamole Capsules in the U.S. Market.
 -Dr. Reddy's Laboratories announces favorable outcome in
 Buprenorphine and Naloxone Sublingual Film patent litigation.
 -Dr. Reddy's Laboratories announces the launch of Atomoxetine
 Capsules, USP in the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Neostigmine
 Methylsulfate Injection, USP in the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Sodium
 Nitroprusside Injection, 50 mg/2 mL (25 mg/mL) Single-dose Vial in
 the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Deferasirox Tablets
 for Oral Suspension, in the U.S. Market.
 -Dr. Reddys Laboratories enters Nutrition Segment with Celevida in
 -Dr. Reddys confirms its voluntary nationwide recall of all
 Ranitidine products in the U.S. Market.
 -Dr. Reddys announces the launch of over-the-counter, store-brand
 equivalent of Prevacid 24HR Capsules (Lansoprazole Delayed-Release
 Capsules USP, 15 mg) in the U.S. Market.
 -Dr. Reddy's Laboratories announces the launch of Vigabatrin Powder
 for Oral Solution, USP in the U.S. Market.
 -Dr. Reddy's Laboratories, Global Response Aid, and Appili
 Therapeutics announce the filing of an application for REEQONUS
 (favipiravir) Tablets for the treatment of COVID-19 under Health
 Canadas Interim Order.
 -Dr. Reddy's and RDIF commence clinical trials for Sputnik V vaccine
 in India.
 -Dr. Reddy's Laboratories announces the launch of Succinylcholine
 Chloride Injection USP, 200 mg/10 mL (20 mg/mL) in the U.S. Market.
 -Dr. Reddy's partners with Department of Biotechnology -
 Biotechnology Industry Research Assistance Council for Sputnik V
 vaccine clinical trials in India.
 -Dr. Reddy's Laboratories announces the launch of a generic version
 of Sapropterin Dihydrochloride Tablets for Oral Use in the U.S.
 -Dr. Reddy's Laboratories receives DCGI approval to launch
 Molnupiravir capsules 200mg (Molflu) in India.
 -Dr. Reddy's Laboratories announces the launch of Venlafaxine ER
 Tablets in the U.S. Market.
 -Dr. Reddy's Laboratories announces approval for Lenalidomide
 Capsules from the U.S. Food and Drug Administration (USFDA).
 -Dr. Reddy's Laboratories Canada announces the launch of
 Reddy-Lenalidomide, one of the first generic medications of its kind
 for the Canadian Market.
 -Dr. Reddy's-ICICI Lombard digital health offering joint.
 - Dr. Reddy's Laboratories announces the launch of Icosapent Ethyl
 Capsules, 1 gram in the U.S. Market