European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
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 1ZHEJIANG CHIRAL MEDICINE CHEMICALS CO., LTD. Hangzhou CN
09 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners 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.
Certificate Number : R1-CEP 2000-331 - Rev 06
Status : Valid
Issue Date : 2014-04-29
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 Etopin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etopin, including repackagers and relabelers. The FDA regulates Etopin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etopin 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 Etopin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etopin supplier is an individual or a company that provides Etopin active pharmaceutical ingredient (API) or Etopin finished formulations upon request. The Etopin suppliers may include Etopin API manufacturers, exporters, distributors and traders.
click here to find a list of Etopin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etopin CEP of the European Pharmacopoeia monograph is often referred to as a Etopin Certificate of Suitability (COS). The purpose of a Etopin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etopin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etopin to their clients by showing that a Etopin CEP has been issued for it. The manufacturer submits a Etopin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etopin CEP holder for the record. Additionally, the data presented in the Etopin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etopin DMF.
A Etopin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etopin 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 Etopin suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Etopin
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