Tini Pharma Limited

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About Us

M/S.TINI PHARMA LTD. was established in the year 1979 by Dr P.R.Reddy (Ramachandra Reddy) and became one of the leading Bulk drugs Manufacturers of Semi-Synthetic penicillin’s (Amoxicillin Trihydrate, Ampicillin Trihydrate, Cloxacillin sodium and Ampicillin Anhydrous) in India.
 
We have been Manufacturing and exporting of penicillin API’s for the past 28 years (1978 -2005 ). From 2006 we renovated the plant for manufacturing the non Penicillin API’s .
Also we started Formulations in 1995 with dedicated manufacturing facilities for Beta-Lactam antibiotics (capsules, tablets, and dry syrups). We start doing contract manufacturing for multinational companies in India and exporting to various countries for the past 16 years. In 1997 we started manufacturing Amoxiclav (co-Amoxiclav) contract manufacturing for Parke-Davis/Pfizer and other multinational companies for Indian market and for export.
 
We have API manufacturing facility and Finished formulations facility based in South India (Tirupati, Andhra Pradesh). Both the facilities are  WHO GMP approved .
 
We are recently ( April -2011 ) tie up with M/s Pharmassyst pvt ltd  to developing R & D on formulation on our facility.



Company Profile
Basic Information
Business Type
  • Manufacturer
  • Exporter
Ownership & Capital
Year of Establishment
1979
Ownership Type
Public Limited Company
Trade & Market
Major Markets
  • Indian Subcontinent
  • East/Middle Africa
  • North Africa
  • South/West Africa
  • East Asia
  • Middle East
  • South East Asia
  • North America
Annual Turnover
US$ 1-10 Million (or Rs. 4-40 Crore Approx.)
Team & Staff
Total Number of Employees
51 to 100 People


Research and Development

M/s TiniPharma Pvt Ltd with the research partner M/s pharmAssyst pvt ltd provides the following the pharmaceutical development services. 
We provide A wide range of pharmaceutical product development services to our clientele encompassing, drug Product registration with the various drug regulatory agencies. Intellectual property management, drug product development services for regulated (USA, EU, Japan, Brazil etc.) and semi-regulated markets. regulatory guidance for Bioequivalence study and Clinical trial related consulting services. With a highly qualified, motivated and experienced team of professionals having an exceptional track record in the areas of Intellectual Property Management, Drug Product Development, API manufacturing and having arguably the highest Bioequivalence study success rate with all the 4 BCS classes of drugs encompassing most therapeutic areas, we believe in providing integrated or custom defined pharmaceutical product development services at a very competent  price within the shortest of timelines thereby drastically reducing the research time and cost for the Client
Contact us
Mr. P. Sasidhar Reddy (Business Development Director)
No. 415, 4th Floor, Nilagiri Block, Aditya Enclave
Hyderabad, Andhra Pradesh - 500 038, India
Telephone:  +(91)-(40)-23737418/ 23734012

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