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Status : Withdrawn by Holder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Status : Withdrawn by Holder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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PharmaCompass also assists you with knowing the Sulfasalazine API Price utilized in the formulation of products. Sulfasalazine API Price is not always fixed or binding as the Sulfasalazine Price is obtained through a variety of data sources. The Sulfasalazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300541 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300541, including repackagers and relabelers. The FDA regulates Tox21_300541 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300541 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 Tox21_300541 supplier is an individual or a company that provides Tox21_300541 active pharmaceutical ingredient (API) or Tox21_300541 finished formulations upon request. The Tox21_300541 suppliers may include Tox21_300541 API manufacturers, exporters, distributors and traders.
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A Tox21_300541 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300541 Certificate of Suitability (COS). The purpose of a Tox21_300541 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300541 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300541 to their clients by showing that a Tox21_300541 CEP has been issued for it. The manufacturer submits a Tox21_300541 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300541 CEP holder for the record. Additionally, the data presented in the Tox21_300541 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300541 DMF.
A Tox21_300541 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300541 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 Tox21_300541 suppliers with CEP (COS) on PharmaCompass.
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