Nectar Lifesciences
BSE: 532649 | NSE: NECLIFE | ISIN: INE023H01027 | Pharmaceuticals
- Directors Report
- Chairman's Speech
- Auditors Report
- Notes To Accounts
- Accounting Policy
- Finished Products
- Raw Materials
| Directors Report | Year End : Mar '08 |
The Directors have pleasure in presenting the 13th Annual Report
together with the audited accounts of Nectar Lifesciences Limited
(Neclife or Nectar or the Company) for the financial year ended
March 31, 2008.
(Rs. in million)
As on March 31, 2008 As on March 31, 2007
Sales and other income 7,874.44 4,873.42
Profit before interest and depreciation 1,384.26 913.97
Interest 273.67 186.98
Depreciation 193.43 104.45
Profit before tax 917.16 622.53
Provision for tax 104.38 64.61
Provision for deferred tax 81.96 73.36
Provision for FBT 1.58 0.98
Income tax relating to earlier years (3.41) (15.43)
MAT credit entitlement (104.38) 63.46)
Profit after tax available for
appropriation 837.03 562.47
Appropriations:
Proposed final dividend 40% (P/Y 20%) 60.90 29.77
Tax on proposed dividend 10.35 5.06
Transfer to general reserve 85.00 57.00
Balance c/f to balance sheet 680.77 470.64
Operations
During the year 2007-08, your Company achieved a sales turnover and
other income of Rs. 7,874.44 mn, registering 61.58% increase over the
previous year (Rs. 4,873.42 mn). Income before interest and
depreciation increased to Rs. 1,384.26 mn, registering 51.46% increase
over the previous year (Rs. 913.97 mn). The net profit increased to Rs.
837.03 mn registering 48.81% increase over the previous year (Rs.
562.47 mn). Your Directors expect a consistent growth in the Companys
performance in the years to come.
The details of the various facilities of the Company are as under.
1. API Facilities
Nectar Lifesciences Limited is one of the leading manufacturers of the
Cephalosporin range of products in India with a leadership in
cephalosporins derived from 7-ACA and GCLE. The Companys core strength
lies in manufacturing oral and sterile APIs, one of the few Indian
companies to enjoy this flexibility. The Company also has
lyophilisation and crystallisation facilities, a distinct edge over its
peers. Neclife possesses world-class API manufacturing facilities built
in compliance with US-FDA guidelines, certified by the WHO GMP and
awarded the ISO 9001:2000 quality management system certification by
DNV Holland.
The Companys principal production facility is located at Derabassi,
Punjab, India and produces oral and sterile forms of Cephalosporins.
Our current API capacity is as follows: Non-steriles: 500 MT/ Annum
Steriles: 250 MT/ Annum Lyophilisation: 50 MT/ Annum Crystalline: 200
MT/ Annum
The Company is a recognised export house by the Indian Director
General of Foreign Trade and also received WHO GMP certificate from the
State Drugs controlling Authority, Directorate of Health And Family
Welfare, Punjab, for its products.
Cephalosporin segment:
Nectars APIs account for about US million and thus hold about 40%
market share in the domestic market and exports in the entire 3rd and
4th generation Cephalosporin segment. Nectar thus is among a few major
integrated Cephalosporin players.
Capacity expansion:
In the current year, Nectar will undergo capacity expansion for
Cefuroxime Axetil by debottlenecking all constraints to increase from
the existing 132 MT/ annum to raise it to 150 MT/ annum. The
additional spray dryer capacity for Axetil Amorphous can be raised to
120 MT/ annum from the existing 50 MT/ annum. This will create an
excess of 60MT/ annum, which Nectar will share with innovator, generic
pharma companies as well as own DMF, which will be filed in the later
half of the year.
Nectar currently has 70% of capacity for Cefixime in the domestic
market with 180 MT/ annum. It also marks a major share in Cefpodoxime
Proxetil with a capacity close to 54 MT/ annum.
The Company aims to file DMF for three products (Phase I) this year
both with US-FDA (US Food & Drug Administration) and EDQM (European
Directorate of Quality & Medicines).
After these filings, the Company expects to get inspected by the
concerned authorities for further approvals and business initiation in
regulated markets.
New products:
Nectar is committed to growth by penetration into new markets, as well
as the introduction of new products in product baskets
Some of the new products to be shortly introduced are:
1) Cefditorin Pivoxil
2) Cefcapene Pivoxil
3) Cefdinir
4) Cefpodoxime Acid
2. Phytochemicals / herbal products
The Company has a wide range of products like menthol crystals (BP/
USP/IP/JP), distilled menthol oil (all grades), peppermint oil,
dementholised peppermint oil, liquid menthol, menthol flakes/ powder,
terpenes, menthones and CIS 3 hexanol.
Till 2007-08, we had two plants, one in Jammu and the other in
Derabassi. As per a market survey conducted by the Company, the market
is expanding by 20-25% per annum and the Company is producing only
about 15% of the total requirement which reflects the huge value to be
unlocked from this sector. Hence, Neclife took an ambitious decision
of ramping up its scale and raise new a state-of-the-art facility,
which marks building of the new facility Unit X, Derabassi. Unit X was
commissioned on April 17, 2008 with additional capacity.
Demand is rising and 2008-09 would see Nectar capturing a strong
foothold in the market with its new facility, hoping to captures
approximately 25% of the global market share, which increased the
production capacity and value-added marketing.
Practically all the other competitors manufacture and market menthol as
a commodity except Nectar which for the first time created a unique
“Pharma Centric” concept. All the products and derivatives made out of
Mentha oil go through a series of cGMP manufacturing practices and
processes followed by very stringent and rigorous quality control &
quality assurance procedures and SOPs. This ensures that our final
product is qualitatively the best in the world available at very
competitive prices.
Nectar will be the only Company to file a US Drug Master File (DMF) in
2008 for pharmaceutical applications of menthol. This will help Nectar
to enhance its realisation of menthol for pharmaceutical applications
in the regulated markets and this will virtually become an assured
business.
3. Empty Hard Gelatine Capsule
The empty hard gelatine capsule unit is located at Baddi, Himachal
Pradesh. Since there is no unit located in the tax- free zone either in
Himachal Pradesh i.e. the state where this facility is located, or in
the adjoining state of Uttaranchal right from day one of production,
the entire production has always been completely sold out at relatively
attractive prices during 2007- 08. Nectar is the only unit in
Uttaranchal and Himachal Pradesh with fiscal benefits being passed on
to the customer along with just-in-time (JIT) delivery. This reduces
the operating cost for customers and secures capsule availability in a
hilly terrain like Baddi. The facility would attain 100% production in
the current year 2008-09 with installation of eighth machine which is
currently under way.
With the first phase of eight high-end automatic machines, the
installed capacity is of producing three billion capsules per annum.
Currently, Nectar is taking trials with the US and Europe- approved
gelatine, which is available at very cost- competitive prices from two
large Indian gelatine manufacturers.
The most critical aspect for qualification for the overseas market is
the compliance of gelatine which is most critical raw material.
The Company will, accordingly, file EHGC DMF for all the markets and in
particular, the regulated markets for the US, Europe and Japan within
the current year and the benefits of this would accrue in the next FY
2009-10. The realisations from regulated markets are very attractive
and the pricing and the bottomline is 1.5-2 times, as compared to the
Indian market.
4. Finished dosage facilities
In Nectar, we possess both dedicated facilities in APIs as well as
formulations on a global scale; the Finished Dosage Form (FDF) facility
is located in Baddi in Himachal Pradesh (India). The facility is
located across five acres i.e. 20000 sq. meters. The Nectar formulation
facility has been designed in such a manner to comply with the cGMP
requirements/guidelines of the US Food & Drug Association (FDA, UK
MHRA, World Health Organisation (WHO), European Union regulations,
Schedule-M requirements of the Indian Drugs & Cosmetics Act and other
relevant regulations.
Aimed at the advanced markets of the US, Europe and other regulated
markets, the facility is well-equipped with the latest sophisticated
equipment to produce and deliver products of high and consistent
quality, adhering to stringent systems and processes for regulatory
compliance. This highly specialised operation is handled by an
experienced team delivering high performance.
The installed production capacities for various Cephalosporin dosage
forms are as under:
Tablets (Coated/ Uncoated): 150 million* Capsules (Hardshell): 150
million* Dry Oral Suspension (Bottles):15 million* Injectables (vials
and amps): 30 million* *Capacity per annum considering single shift per
day.
Since Nectar is into high-quality APIs in GMP-compliant facility, the
FDF venture is a logical step and completes its forward integration,
acting as a one-stop for all our customers.
We have got firm contracts and commitments with six top Indian pharma
companies for manufacturing brands which were hitherto manufactured by
our competitors, who undertake similar Principle to Principle (P2P)
business both in the oral and sterile formulations of Cephalosporins.
We have a unique position in the market with a differentiated value
proposition and a robust business model. Currently in this P2P
business, we stand out to be the best available partner for leading
most domestic players, due to our core strengths:
1) Best available infrastructure in industry.
2) QA support with USFDA compliant facility for domestic players.
Nectar will file two ANDAs (Abbreviated New DRUG Applications) in
regulated markets of both USFDA and ECTD in the current year; many more
are planned in a phased manner for the next year. As a way to enter the
semi-regulated markets or ROW markets, Nectar will file almost close to
50 or more dossiers, followed by registration in those countries.
5. Captive power plant
The Company has put up an agro-based captive power generation plant at
Derabassi (Unit II) which runs on husk and can be switched over to wood
chips, saw dust, leaf cuttings, etc., with a capacity to generate 6-MW
electricity power. The in-house captive power plant (co-generation of
steam) commenced during Q2, 2007 has a tremendous energy saving
potential for the Company. The energy bill is poised to reduce by 20%.
6. Corporate Quality Control and Research and Development Centre
R&D is a vital and the backbone of every growing organisation, driving
it towards innovation, project planning and implementation. To meet the
R&D challenges in this industry, Neclife has set up an ultra-modern R&D
centre to support the manufacturing facilities at Derabassi Unit II.
Key prominent features of R&D are:
- Ever-improving production processes being developed to obtain better
yield and quality parameters.
- State-of-the-art facility with requisite instruments.
- Strong process development R&D capabilities.
- Qualified scientists including PhDs and post graduates in analytical
chemistry include patent holders in the Cephalosporin range
Since R&D activities are done on a regular basis, more improvements and
reduction in the cost in production would follow in with the passage of
time.
During the year, our R&D has developed the following technologies:
1) NIP (Non-infringing route) for Cefuroxime Axetil DMF filling
2) NIP for Ceftriaxone Na
3) NIP for Cefixime Trihydrate
Nectar aims to file for all the above DMFs in the current fiscal year.
Through dedicated QA/QC cell and stringent quality parameters and
checks, we have tremendously reduced customer rejections and customer
complaints. Due to a focused and quality-centric approach, Nectar has
been successful to retain key clients, in spite of heavy competition
and has in fact broadened the customer base manifold.
We had witnessed some successful audits from big customers during this
year, who have committed and signed on dotted lines for continuous
business in the times to come both in API, FDF and phytochemicals.
Foreign Currency Convertible Bonds
The Company has raised funds to the tune of US,000,000 by way of
Foreign Currency Convertible Bonds (FCCBs), on 25.04.2006. The details
of utilisation of such proceeds are disclosed to the Audit Committee.
The Company has utilised these funds for purposes as stated in the
Notice for convening the Extraordinary General Meeting held on
15.12.2005, vide which approval of Members has been received for the
issue of the said FCCBs. During the year, the conversion price has been
adjusted to Rs. 263.22 w.e.f. 20.09.2007, upon declaration of the final
dividend of 20% by the members in their Annual General Meeting held on
28.09.2007.
The Allotment Committee in its meeting held on 07.01.2008 has allotted
339,430 equity shares of Rs. 10 each, upon conversion of Zero Coupon
Convertible Bonds due 2011 (FCCBs) of US$ 2,000,000. Consequently, the
paid-up equity share capital stand increased from Rs. 148,866,670
(comprising 14,886,667 equity shares of Rs. 10 each) to Rs. 152,260,970
(comprising 15,226,097 equity shares of Rs. 10 each.
The equity share capital of the Company would further increase by
5,600,609 equity shares to 20,826,706 equity shares, if the balance
FCCBs of US million are converted at an adjusted price of Rs. 263.22
at a predetermined exchange rate of US = Rs. 44.6725.
Subsidiary Company
The Company has the wholly owned subsidiary M/s Chempharma Private
Limited incorporated in Sri Lanka. The operations of the said
subsidiary remain suspended throughout the year and your Directors have
decided to wind up its operations, because of its profitability in
changed circumstances.
A copy of Balance Sheet, a copy of Profit & Loss Account, a copy of
Directors Report and a copy of Auditors report of its subsidiary
company is attached. However, the statement pursuant to Section 212 of
the Companies Act, 1956, in respect of the subsidiary is given on the
next page:
1. Name of Subsidiary M/s Chempharma Private Limited
2. Financial year of subsidiary ended on March 31, 2008
3. Date from which it become subsidiary October 18, 2002
4. Shares of subsidiary held by the Company as on 31.03.2008:
a. Number and face value 9,614,165 shares of SLR. 10/- each
b. Extent of holding 100%
5. The net aggregate amount of subsidiary companys profit (loss) so
for as it concerns the members of holding company
a. Not dealt with in holding companys accounts
i. For the financial year ended 31.03.2008 (Rs. 36/-)
ii. Up to previous financial year of the subsidiary company Rs. 54/-
b. Dealt with in holding companys accounts
i. For the financial year ended 31.03.2008 Rs. 1,992,828/-
ii. Up to previous financial year of the subsidiary company Rs.
7,889,531/-
Consolidated financial results
As required under the Listing Agreement with the stock exchanges, the
consolidated financial statements for the year ended on 31.03.2008 of
the Company are attached. The consolidated financial statements include
the financial statements of Nectar Lifesciences Limited, the parent
Company and its subsidiary Company Chempharma (Private) Limited, Sri
Lanka.
Dividend
During the current financial year, the Board of Directors has
recommended the final dividend at 40% i.e. Rs. 4 per equity share
aggregating to Rs. 60,904,388 of the Company, subject to the approval
by the shareholders in the forthcoming Annual General Meeting. After
the approval of the shareholders at the ensuing Annual General Meeting,
the dividend would be paid to those shareholders, whose names appear on
the Register of members as on 19.09.2008.
As per the requirements of Section 205(2A) of the Companies Act, 1956,
read with the Companies (Transfer of Profit to Reserve) Rules, 1975,
your Directors proposed to transfer an amount of Rs. 85,000,000 from
the net profit to the general reserve account.
Directors
Mrs. Raman Goyal has resigned from the Board on June 20, 2008. The
Board while accepting her resignation recorded her contribution during
her tenure on the Board with appreciation.
Further, on June 20, 2008, Mr. Saurabh Goyal has been appointed as
Additional Director and vacates his office at the ensuing Annual
General Meeting. However, the Company has received a notice under
Section 257 of the Companies Act, 1956, from a member signifying his
intention to propose the candidature of Mr. Saurabh Goyal as a Regular
Director of the Company. Further, Mr. Saurabh Goyal has also been
appointed as an Executive Director, subject to the approval of the
shareholders in their General Meeting. Thus, your Directors recommend
his appointment as a regular as well as Executive Director.
Dr. S. P. Singh retires by rotation and being eligible, offers himself
for re-appointment. The Board recommends his re- appointment.
Directors responsibility statement
Pursuant to the requirement under Section 217(2AA) of the Companies
Act, 1956, with respect to the Directors Responsibility Statement,
your Directors confirm:
(i) That in the preparation of the accounts for the financial year
ended March 31, 2008, the applicable accounting standards have been
followed along with proper explanation relating to material departures,
if any;
(ii) That the Directors have selected such accounting policies and
applied them consistently and made judgements and estimates that were
reasonable and prudent, so as to give a true and fair view of the state
of affairs of the Company at the end of the financial year and of the
profit or loss of the Company for the year under review;
(iii) That the Directors have taken proper and sufficient care for the
maintenance of adequate accounting records in accordance with the
provisions of the Companies Act, 1956 for safeguarding the assets of
the Company and for preventing and detecting fraud and other
irregularities; and
(iv) That the Directors have prepared the accounts for the financial
year ended March 31, 2008 on a `going concern basis.
Auditors
M/s Datta Singla & Co., chartered accountants, statutory auditors of
the Company retire at the conclusion of the forthcoming Annual General
Meeting and being eligible, offer themselves for re-appointment.
The Audit Committee and Board of Directors recommend their
re-appointment as auditors.
Auditors Report
Observations made in the Auditors Report are self-explanatory and
therefore do not call for any further comments.
Audit Committee
The Company has constituted the Audit Committee as per the provisions
of Section 292A of the Companies Act, 1956 and Clause 49 of the Listing
Agreement. The composition, powers and duties of the Audit Committee
are detailed out in the Corporate Governance Report. The Board of
Directors has accepted all recommendations of the Audit committee.
Energy, Technology and Foreign Exchange
Information required under Section 217(1)(e) of the Companies Act,
1956, read with the Companies (Disclosure of Particulars in the Report
of Board of Directors) Rules, 1988, with respect to conservation of
energy, technology absorption and foreign exchange earnings and outgo
are given in Annexure I and form part of this report.
Personnel
Information pursuant to Section 217(2A) of the Companies Act, 1956,
read with the Companies (Particulars of Employees) Rules, 1975, as
amended, form part of the report. However, as per the provisions of
Section 219(1)(b)(iv) of the Companies Act, 1956, the report and
accounts are being sent to the shareholders, excluding statement of
particulars of employees under Section 217(2A) of the act. Any
shareholder interested in obtaining the copy of the said statement may
write to the Secretarial Department at the corporate office of the
Company.
The Company enjoyed cordial relations with its employees at all levels.
Fixed Deposits
During the year under report, your Company did not accept any deposits
from the public in terms the provisions of Sections 58A and 58AA of the
Companies Act, 1956.
Corporate Governance
The Company has aimed to conduct its affairs in an ethical manner. A
separate report on Corporate Governance forms a part of the annual
report. A certificate from the auditors of the Company regarding the
compliance of conditions of Corporate Governance as stipulated under
Clause 49 of the Listing Agreement is given in Annexure II.
Management Discussion and Analysis Report
Management discussion and analysis of the financial condition and
results of operations of the Company for the financial year 2007-08 as
required under Clause 49 of the Listing Agreement with the stock
exchanges is given as a separate statement in the Annual Report.
Acknowledgement
Your Directors would like to express their sincere and grateful
appreciation for the assistance and co-operation received from the
bankers and government authorities and also thank the shareholders for
the confidence reposed by them in the Company and look forward to their
valuable support in the future plans of the Company.
Your Directors also thank its agents, the medical professionals and its
customers for their continued patronage to the Companys products.
For and on behalf of the Board of Directors
of Nectar Lifesciences Limited
Chandigarh Sanjiv Goyal
June 20, 2008 Chairman & Managing Director
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