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 Petach Tikva IL
02 1CIPLA LIMITED Mumbai IN
03 1JIANGSU HENGRUI PHARMACEUTICALS CO., LTD. Lianyungang CN
04 1MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN
05 1NIPPON KAYAKU CO., LTD. Tokyo JP
06 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
07 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 7Etoposide
01 2China
02 2India
03 2Israel
04 1Japan
01 5Valid
02 2Withdrawn 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 : R1-CEP 1997-126 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2009-10-27
Type : Chemical
Substance Number : 823
Certificate Number : CEP 2007-061 - Rev 06
Status : Valid
Issue Date : 2024-09-17
Type : Chemical
Substance Number : 823
Certificate Number : CEP 2008-037 - Rev 05
Status : Valid
Issue Date : 2023-10-09
Type : Chemical
Substance Number : 823
Certificate Number : CEP 2020-074 - Rev 01
Status : Valid
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 823
Certificate Number : R1-CEP 2004-003 - Rev 03
Status : Valid
Issue Date : 2015-08-12
Type : Chemical
Substance Number : 823
Certificate Number : R0-CEP 2010-119 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-10-06
Type : Chemical
Substance Number : 823
Certificate Number : R1-CEP 1999-144 - Rev 07
Status : Valid
Issue Date : 2022-01-04
Type : Chemical
Substance Number : 823
A Etoposide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etoposide, including repackagers and relabelers. The FDA regulates Etoposide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etoposide 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 Etoposide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etoposide supplier is an individual or a company that provides Etoposide active pharmaceutical ingredient (API) or Etoposide finished formulations upon request. The Etoposide suppliers may include Etoposide API manufacturers, exporters, distributors and traders.
click here to find a list of Etoposide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etoposide CEP of the European Pharmacopoeia monograph is often referred to as a Etoposide Certificate of Suitability (COS). The purpose of a Etoposide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etoposide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etoposide to their clients by showing that a Etoposide CEP has been issued for it. The manufacturer submits a Etoposide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etoposide CEP holder for the record. Additionally, the data presented in the Etoposide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etoposide DMF.
A Etoposide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etoposide 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 Etoposide suppliers with CEP (COS) on PharmaCompass.
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