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01 1CSPC OUYI PHARMACEUTICAL CO., LTD. Shijiazhuang CN
02 1ESTEVE QUIMICA S.A. Barcelona ES
03 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
04 1HETERO DRUGS LIMITED Hyderabad IN
05 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
06 1YUNPENG PHARMACEUTICAL GROUP CO., LTD. Linfen City CN
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01 5Indometacin
02 1Indometacin, Micronised, non-micronised
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01 2China
02 2India
03 1Italy
04 1Spain
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01 5Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2008-004 - Rev 07
Status : Valid
Issue Date : 2025-01-22
Type : Chemical
Substance Number : 92
Certificate Number : R1-CEP 1997-006 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2020-10-28
Type : Chemical
Substance Number : 92
Indometacin, Micronised, Non-micronised
Certificate Number : R1-CEP 2009-256 - Rev 03
Status : Valid
Issue Date : 2023-01-25
Type : Chemical
Substance Number : 92
Certificate Number : R0-CEP 2022-003 - Rev 00
Status : Valid
Issue Date : 2023-03-31
Type : Chemical
Substance Number : 92
Certificate Number : R1-CEP 2009-314 - Rev 00
Status : Valid
Issue Date : 2016-04-07
Type : Chemical
Substance Number : 92
Certificate Number : CEP 2021-484 - Rev 00
Status : Valid
Issue Date : 2024-06-04
Type : Chemical
Substance Number : 92
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PharmaCompass offers a list of Indomethacin 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 Indomethacin manufacturer or Indomethacin supplier for your needs.
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PharmaCompass also assists you with knowing the Indomethacin API Price utilized in the formulation of products. Indomethacin API Price is not always fixed or binding as the Indomethacin Price is obtained through a variety of data sources. The Indomethacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arthrexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arthrexin, including repackagers and relabelers. The FDA regulates Arthrexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arthrexin 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 Arthrexin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arthrexin supplier is an individual or a company that provides Arthrexin active pharmaceutical ingredient (API) or Arthrexin finished formulations upon request. The Arthrexin suppliers may include Arthrexin API manufacturers, exporters, distributors and traders.
click here to find a list of Arthrexin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Arthrexin CEP of the European Pharmacopoeia monograph is often referred to as a Arthrexin Certificate of Suitability (COS). The purpose of a Arthrexin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Arthrexin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Arthrexin to their clients by showing that a Arthrexin CEP has been issued for it. The manufacturer submits a Arthrexin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Arthrexin CEP holder for the record. Additionally, the data presented in the Arthrexin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Arthrexin DMF.
A Arthrexin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Arthrexin 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 Arthrexin suppliers with CEP (COS) on PharmaCompass.
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