TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
02 1Teva Group - Bulk Pharmaceutical Chemicals Division Petah Tiqva IL
03 1ALBANY MOLECULAR RESEARCH HYDERABAD RESEARCH CENTRE PRIVATE LIMITED Hyderabad IN
04 1Cosma S.p.A. Ciserano IT
05 1IPCA LABORATORIES LIMITED Mumbai IN
06 2KOPRAN RESEARCH LABORATORIES LIMITED Mumbai IN
07 1MYLAN LABORATORIES LIMITED Hyderabad IN
08 1PHARMAZELL (INDIA) PRIVATE LIMITED Chennai IN
09 1Unique Chemicals (A Division of J.B. Chemicals & Pharmaceuticals Ltd.) Mumbai IN
10 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
01 10Atenolol
02 1Atenolol, ALA route
01 6India
02 2Israel
03 1Italy
04 2U.S.A
01 1Expired
02 6Valid
03 4Withdrawn by Holder
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2004-030 - Rev 08
Status : Valid
Issue Date : 2024-03-06
Type : Chemical
Substance Number : 703
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R0-CEP 1998-033 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2002-05-02
Type : Chemical
Substance Number : 703
Certificate Number : R0-CEP 2001-426 - Rev 01
Status : Expired
Issue Date : 2004-10-22
Type : Chemical
Substance Number : 703
Certificate Number : CEP 1998-024 - Rev 06
Status : Valid
Issue Date : 2023-11-10
Type : Chemical
Substance Number : 703
Certificate Number : R1-CEP 2016-226 - Rev 00
Status : Valid
Issue Date : 2023-05-02
Type : Chemical
Substance Number : 703
Certificate Number : R0-CEP 2021-479 - Rev 00
Status : Valid
Issue Date : 2022-07-27
Type : Chemical
Substance Number : 703
Certificate Number : CEP 1998-017 - Rev 07
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 703
Certificate Number : R0-CEP 2007-306 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2011-11-08
Type : Chemical
Substance Number : 703
Certificate Number : R1-CEP 2005-093 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-09-30
Type : Chemical
Substance Number : 703
Certificate Number : R1-CEP 2004-169 - Rev 04
Status : Valid
Issue Date : 2022-07-07
Type : Chemical
Substance Number : 703
A Tenormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenormin, including repackagers and relabelers. The FDA regulates Tenormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenormin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tenormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenormin supplier is an individual or a company that provides Tenormin active pharmaceutical ingredient (API) or Tenormin finished formulations upon request. The Tenormin suppliers may include Tenormin API manufacturers, exporters, distributors and traders.
click here to find a list of Tenormin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenormin CEP of the European Pharmacopoeia monograph is often referred to as a Tenormin Certificate of Suitability (COS). The purpose of a Tenormin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tenormin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tenormin to their clients by showing that a Tenormin CEP has been issued for it. The manufacturer submits a Tenormin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tenormin CEP holder for the record. Additionally, the data presented in the Tenormin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tenormin DMF.
A Tenormin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tenormin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Tenormin suppliers with CEP (COS) on PharmaCompass.
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