Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
03 1TEVA PHARMACEUTICAL INDUSTRIES LTD. Petach Tikva IL
04 1FLEMING LABORATORIES LIMITED Nawabpet Village IN
05 1IPCA LABORATORIES LIMITED Mumbai IN
06 1KREATIVE ORGANICS PRIVATE LIMITED Hyderabad IN
07 1MITRYCHEM S.A.S. Mitry-Mory FR
08 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
09 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
10 1Zhejiang Chiral Medicine Chemicals Co., Ltd. Hangzhou CN
01 7Etodolac
02 1Etodolac, Micronised
03 2Etodolac, Micronised, non-micronised
01 1China
02 1France
03 4India
04 1Israel
05 2Poland
06 1U.S.A
01 1Expired
02 1VALID
03 8Valid
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2013-134 - Rev 02
Status : VALID
Issue Date : 2023-02-07
Type : Chemical
Substance Number : 1422
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 2000-331 - Rev 06
Status : Valid
Issue Date : 2014-04-29
Type : Chemical
Substance Number : 1422
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Etodolac, Micronised, Non-micronised
Certificate Number : CEP 2013-134 - Rev 03
Status : Valid
Issue Date : 2024-12-02
Type : Chemical
Substance Number : 1422
Certificate Number : R1-CEP 2015-180 - Rev 00
Status : Valid
Issue Date : 2023-05-02
Type : Chemical
Substance Number : 1422
Certificate Number : CEP 2008-175 - Rev 04
Status : Valid
Issue Date : 2023-09-21
Type : Chemical
Substance Number : 1422
Certificate Number : CEP 2014-131 - Rev 01
Status : Valid
Issue Date : 2024-08-26
Type : Chemical
Substance Number : 1422
Certificate Number : R0-CEP 2013-084 - Rev 01
Status : Expired
Issue Date : 2015-02-13
Type : Chemical
Substance Number : 1422
Certificate Number : R1-CEP 2004-082 - Rev 06
Status : Valid
Issue Date : 2023-04-03
Type : Chemical
Substance Number : 1422
Etodolac, Micronised, Non-micronised
Certificate Number : CEP 2009-338 - Rev 03
Status : Valid
Issue Date : 2024-10-29
Type : Chemical
Substance Number : 1422
Certificate Number : R1-CEP 2017-017 - Rev 00
Status : Valid
Issue Date : 2023-01-19
Type : Chemical
Substance Number : 1422
A Etodolac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etodolac, including repackagers and relabelers. The FDA regulates Etodolac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etodolac 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 Etodolac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etodolac supplier is an individual or a company that provides Etodolac active pharmaceutical ingredient (API) or Etodolac finished formulations upon request. The Etodolac suppliers may include Etodolac API manufacturers, exporters, distributors and traders.
click here to find a list of Etodolac suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etodolac CEP of the European Pharmacopoeia monograph is often referred to as a Etodolac Certificate of Suitability (COS). The purpose of a Etodolac CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etodolac EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etodolac to their clients by showing that a Etodolac CEP has been issued for it. The manufacturer submits a Etodolac CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etodolac CEP holder for the record. Additionally, the data presented in the Etodolac CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etodolac DMF.
A Etodolac CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etodolac 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 Etodolac suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Etodolac
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