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 HISOAR PHARMACEUTICAL CO., LTD. Taizhou CN
06 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
01 6Sulfasalazine
01 3China
02 1India
03 1Italy
04 1U.S.A
01 1Expired
02 3Valid
03 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Status : Withdrawn by Holder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Status : Withdrawn by Holder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 : R0-CEP 2015-073 - Rev 02
Status : Expired
Issue Date : 2020-01-06
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 Azulfidine EN-tabs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azulfidine EN-tabs, including repackagers and relabelers. The FDA regulates Azulfidine EN-tabs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azulfidine EN-tabs 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 Azulfidine EN-tabs supplier is an individual or a company that provides Azulfidine EN-tabs active pharmaceutical ingredient (API) or Azulfidine EN-tabs finished formulations upon request. The Azulfidine EN-tabs suppliers may include Azulfidine EN-tabs API manufacturers, exporters, distributors and traders.
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A Azulfidine EN-tabs CEP of the European Pharmacopoeia monograph is often referred to as a Azulfidine EN-tabs Certificate of Suitability (COS). The purpose of a Azulfidine EN-tabs CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Azulfidine EN-tabs EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Azulfidine EN-tabs to their clients by showing that a Azulfidine EN-tabs CEP has been issued for it. The manufacturer submits a Azulfidine EN-tabs CEP (COS) as part of the market authorization procedure, and it takes on the role of a Azulfidine EN-tabs CEP holder for the record. Additionally, the data presented in the Azulfidine EN-tabs CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Azulfidine EN-tabs DMF.
A Azulfidine EN-tabs CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Azulfidine EN-tabs 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 Azulfidine EN-tabs suppliers with CEP (COS) on PharmaCompass.
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