Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 1TEVA PHARMACEUTICAL INDUSTRIES LTD. Petach Tikva IL
03 1FLEMING LABORATORIES LIMITED Nawabpet Village IN
04 1IPCA LABORATORIES LIMITED Mumbai IN
05 1KREATIVE ORGANICS PRIVATE LIMITED Hyderabad IN
06 1MITRYCHEM S.A.S. Mitry-Mory FR
07 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
08 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
09 1Zhejiang Chiral Medicine Chemicals Co., Ltd. Hangzhou CN
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01 6Etodolac
02 1Etodolac, Micronised
03 2Etodolac, Micronised, non-micronised
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01 1China
02 1France
03 4India
04 1Israel
05 1Poland
06 1U.S.A
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01 1Expired
02 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.
Etodolac, Micronised, Non-micronised
Certificate Number : CEP 2013-134 - Rev 03
Status : Valid
Issue Date : 2024-12-02
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
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
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PharmaCompass offers a list of Etodolac API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Etodolac manufacturer or Etodolac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etodolac manufacturer or Etodolac supplier.
PharmaCompass also assists you with knowing the Etodolac API Price utilized in the formulation of products. Etodolac API Price is not always fixed or binding as the Etodolac Price is obtained through a variety of data sources. The Etodolac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etodolac, (S)-Isomer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etodolac, (S)-Isomer, including repackagers and relabelers. The FDA regulates Etodolac, (S)-Isomer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etodolac, (S)-Isomer 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, (S)-Isomer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etodolac, (S)-Isomer supplier is an individual or a company that provides Etodolac, (S)-Isomer active pharmaceutical ingredient (API) or Etodolac, (S)-Isomer finished formulations upon request. The Etodolac, (S)-Isomer suppliers may include Etodolac, (S)-Isomer API manufacturers, exporters, distributors and traders.
click here to find a list of Etodolac, (S)-Isomer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etodolac, (S)-Isomer CEP of the European Pharmacopoeia monograph is often referred to as a Etodolac, (S)-Isomer Certificate of Suitability (COS). The purpose of a Etodolac, (S)-Isomer CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etodolac, (S)-Isomer EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etodolac, (S)-Isomer to their clients by showing that a Etodolac, (S)-Isomer CEP has been issued for it. The manufacturer submits a Etodolac, (S)-Isomer CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etodolac, (S)-Isomer CEP holder for the record. Additionally, the data presented in the Etodolac, (S)-Isomer CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etodolac, (S)-Isomer DMF.
A Etodolac, (S)-Isomer CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etodolac, (S)-Isomer 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, (S)-Isomer suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Etodolac, (S)-Isomer
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