01 1CAMBREX CHARLES CITY, INC. Charles City US
02 1CORDEN PHARMA BERGAMO S.P.A. Treviglio IT
03 1JIANGSU RUIKE PHARMACEUTICAL SCI-TECH CO., LTD. Yancheng City CN
04 1VALENS MOLECULES PRIVATE LIMITED Hyderabad IN
05 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
01 5Sulfasalazine
01 2China
02 1India
03 1Italy
04 1U.S.A
01 3Valid
02 2Withdrawn by Holder
Certificate Number : R1-CEP 1996-040 - Rev 02
Status : Valid
Issue Date : 2007-08-30
Type : Chemical
Substance Number : 863
Certificate Number : R1-CEP 2004-278 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2017-12-20
Type : Chemical
Substance Number : 863
Certificate Number : R1-CEP 2016-225 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2022-01-10
Type : Chemical
Substance Number : 863
Certificate Number : R1-CEP 2016-085 - Rev 00
Status : Valid
Issue Date : 2023-01-19
Type : Chemical
Substance Number : 863
Certificate Number : R1-CEP 2002-088 - Rev 02
Status : Valid
Issue Date : 2015-03-20
Type : Chemical
Substance Number : 863
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PharmaCompass offers a list of Sulfasalazine 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 Sulfasalazine manufacturer or Sulfasalazine supplier for your needs.
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A Prestwick3_000520 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000520, including repackagers and relabelers. The FDA regulates Prestwick3_000520 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000520 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Prestwick3_000520 supplier is an individual or a company that provides Prestwick3_000520 active pharmaceutical ingredient (API) or Prestwick3_000520 finished formulations upon request. The Prestwick3_000520 suppliers may include Prestwick3_000520 API manufacturers, exporters, distributors and traders.
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A Prestwick3_000520 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_000520 Certificate of Suitability (COS). The purpose of a Prestwick3_000520 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_000520 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_000520 to their clients by showing that a Prestwick3_000520 CEP has been issued for it. The manufacturer submits a Prestwick3_000520 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_000520 CEP holder for the record. Additionally, the data presented in the Prestwick3_000520 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_000520 DMF.
A Prestwick3_000520 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_000520 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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