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01 1PharmaZell GmbH Raubling DE
02 2ZHEJIANG HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
03 2A.H.A International Co., Ltd. Hefei CN
04 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
05 1BAYER AG Leverkusen DE
06 2BEC CHEMICALS PRIVATE LIMITED Mumbai IN
07 2CAMBREX KARLSKOGA AB Karlskoga SE
08 2CHEMI S.P.A. Patrica IT
09 2CORDEN PHARMA BERGAMO S.P.A. Treviglio IT
10 1CTX LIFESCIENCES PVT. LIMITED Surat IN
11 1DIVI'S LABORATORIES LIMITED Hyderabad IN
12 2Erregierre S.p.A. San Paolo D'Argon IT
13 1HY-GRO CHEMICALS PHARMTEK PRIVATE LIMITED Secunderabad IN
14 2IPCA Laboratories Limited Mumbai IN
15 1JIANGSU JUBANG PHARMACEUTICAL CO., LTD. Liyang CN
16 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
17 1MERCK & CIE KMG Schaffhausen CH
18 1PLIVA CROATIA LTD. Zagreb HR
19 1S.A. AJINOMOTO OMNICHEM N.V. Louvain-La-Neuve BE
20 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
21 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
22 2Syntese A/S Hvidovre DK
23 1ZHEJIANG SANMEN HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
24 2ZYDUS LIFESCIENCES LIMITED Vadodara IN
01 21Mesalazine
02 1Mesalazine, Grade S
03 1Mesalazine, Grade SH
04 1Mesalazine, HP
05 2Mesalazine, High density
06 1Mesalazine, Mesalazine (MZ4B Process)
07 2Mesalazine, Micronised
08 1Mesalazine, Process-I
09 1Mesalazine, Product codes: FV0945, FV0945C, FV0947 and FV0947C
10 1Mesalazine, Products codes: FV 0950 (milled), FV 0950C (milled), FV 0945D (milled), FV 0941 (high bulk density), FV 0941C (high bulk density), FV 0941A (high bulk density), FV 0941AC (high bulk density), FV 0941S (high bulk density), FV 0941SC (high bulk
11 1Mesalazine, Pubagang site
12 1Mesalazine, Regular density
13 1Mesalazine, Site II
01 6China
02 1Croatia
03 2Denmark
04 2Germany
05 14India
06 6Italy
07 1Japan
08 1Switzerland
09 2U.S.A
01 2Expired
02 27Valid
03 6Withdrawn by Holder
Certificate Number : CEP 2003-203 - Rev 03
Status : Valid
Issue Date : 2023-11-08
Type : Chemical
Substance Number : 1699
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Certificate Number : R0-CEP 2021-400 - Rev 00
Status : Valid
Issue Date : 2021-12-17
Type : Chemical
Substance Number : 1699
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Certificate Number : R1-CEP 2015-209 - Rev 00
Status : Valid
Issue Date : 2021-05-06
Type : Chemical
Substance Number : 1699
Certificate Number : R1-CEP 2011-100 - Rev 00
Status : Valid
Issue Date : 2017-06-29
Type : Chemical
Substance Number : 1699
Certificate Number : R1-CEP 2015-152 - Rev 00
Status : Valid
Issue Date : 2021-06-09
Type : Chemical
Substance Number : 1699
Certificate Number : R1-CEP 2006-122 - Rev 04
Status : Valid
Issue Date : 2019-12-05
Type : Chemical
Substance Number : 1699
Certificate Number : R1-CEP 2012-162 - Rev 00
Status : Valid
Issue Date : 2019-03-11
Type : Chemical
Substance Number : 1699
Certificate Number : R1-CEP 2016-246 - Rev 00
Status : Valid
Issue Date : 2022-04-08
Type : Chemical
Substance Number : 1699
Certificate Number : CEP 2004-056 - Rev 06
Status : Valid
Issue Date : 2024-03-04
Type : Chemical
Substance Number : 1699
Certificate Number : CEP 2024-395 - Rev 00
Status : Valid
Issue Date : 2024-11-13
Type : Chemical
Substance Number : 1699
A CAS-89-57-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-89-57-6, including repackagers and relabelers. The FDA regulates CAS-89-57-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-89-57-6 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 CAS-89-57-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-89-57-6 supplier is an individual or a company that provides CAS-89-57-6 active pharmaceutical ingredient (API) or CAS-89-57-6 finished formulations upon request. The CAS-89-57-6 suppliers may include CAS-89-57-6 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-89-57-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CAS-89-57-6 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-89-57-6 Certificate of Suitability (COS). The purpose of a CAS-89-57-6 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-89-57-6 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-89-57-6 to their clients by showing that a CAS-89-57-6 CEP has been issued for it. The manufacturer submits a CAS-89-57-6 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-89-57-6 CEP holder for the record. Additionally, the data presented in the CAS-89-57-6 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-89-57-6 DMF.
A CAS-89-57-6 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-89-57-6 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 CAS-89-57-6 suppliers with CEP (COS) on PharmaCompass.
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