01 1Indosol Drugs Limited Mumbai IN
02 1SHOUGUANG FUKANG PHARMACEUTICAL CO., LTD. Shouguang City CN
03 1SOUTHWEST SYNTHETIC PHARMACEUTICAL CORPORATION, LIMITED Chongqing CN
04 1Virchow Laboratories Limited Hyderabad IN
01 4Sulfamethoxazole
01 2China
02 2India
01 2Valid
02 2Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 1998-049 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2004-02-01
Type : Chemical
Substance Number : 108
Certificate Number : R1-CEP 2007-332 - Rev 01
Status : Valid
Issue Date : 2017-07-11
Type : Chemical
Substance Number : 108
Certificate Number : R1-CEP 1999-097 - Rev 03
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2015-12-08
Type : Chemical
Substance Number : 108
Certificate Number : R1-CEP 1999-172 - Rev 02
Status : Valid
Issue Date : 2019-10-10
Type : Chemical
Substance Number : 108
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PharmaCompass offers a list of Sulfamethoxazole 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 Sulfamethoxazole manufacturer or Sulfamethoxazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfamethoxazole manufacturer or Sulfamethoxazole supplier.
PharmaCompass also assists you with knowing the Sulfamethoxazole API Price utilized in the formulation of products. Sulfamethoxazole API Price is not always fixed or binding as the Sulfamethoxazole Price is obtained through a variety of data sources. The Sulfamethoxazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SEPTRA DS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SEPTRA DS, including repackagers and relabelers. The FDA regulates SEPTRA DS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SEPTRA DS 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 SEPTRA DS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SEPTRA DS supplier is an individual or a company that provides SEPTRA DS active pharmaceutical ingredient (API) or SEPTRA DS finished formulations upon request. The SEPTRA DS suppliers may include SEPTRA DS API manufacturers, exporters, distributors and traders.
click here to find a list of SEPTRA DS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SEPTRA DS CEP of the European Pharmacopoeia monograph is often referred to as a SEPTRA DS Certificate of Suitability (COS). The purpose of a SEPTRA DS CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of SEPTRA DS EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of SEPTRA DS to their clients by showing that a SEPTRA DS CEP has been issued for it. The manufacturer submits a SEPTRA DS CEP (COS) as part of the market authorization procedure, and it takes on the role of a SEPTRA DS CEP holder for the record. Additionally, the data presented in the SEPTRA DS CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the SEPTRA DS DMF.
A SEPTRA DS CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. SEPTRA DS 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 SEPTRA DS suppliers with CEP (COS) on PharmaCompass.
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