01 1NANHAI BEISHA PHARMACEUTICAL CO., LTD. Foshan City CN
02 1SCHMITT PHARMA GMBH Kleinmachnow DE
03 1SOUTHWEST SYNTHETIC PHARMACEUTICAL CORPORATION, LIMITED Chongqing CN
01 3Sulfadimidine
01 2China
02 1Blank
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 2001-261 - Rev 01
Status : Valid
Issue Date : 2020-07-28
Type : Chemical
Substance Number : 295
Certificate Number : R1-CEP 1995-039 - Rev 06
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2015-12-08
Type : Chemical
Substance Number : 295
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Certificate Number : CEP 2023-258 - Rev 00
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 295
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Product Web Link
Virtual Booth
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Website
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PharmaCompass offers a list of Sulfadimidine 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 Sulfadimidine manufacturer or Sulfadimidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfadimidine manufacturer or Sulfadimidine supplier.
PharmaCompass also assists you with knowing the Sulfadimidine API Price utilized in the formulation of products. Sulfadimidine API Price is not always fixed or binding as the Sulfadimidine Price is obtained through a variety of data sources. The Sulfadimidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Superseptyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Superseptyl, including repackagers and relabelers. The FDA regulates Superseptyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Superseptyl 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 Superseptyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Superseptyl supplier is an individual or a company that provides Superseptyl active pharmaceutical ingredient (API) or Superseptyl finished formulations upon request. The Superseptyl suppliers may include Superseptyl API manufacturers, exporters, distributors and traders.
click here to find a list of Superseptyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Superseptyl CEP of the European Pharmacopoeia monograph is often referred to as a Superseptyl Certificate of Suitability (COS). The purpose of a Superseptyl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Superseptyl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Superseptyl to their clients by showing that a Superseptyl CEP has been issued for it. The manufacturer submits a Superseptyl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Superseptyl CEP holder for the record. Additionally, the data presented in the Superseptyl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Superseptyl DMF.
A Superseptyl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Superseptyl 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 Superseptyl suppliers with CEP (COS) on PharmaCompass.
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