01 1Albert David Ltd Calcutta IN
02 1Kothari Phytochemicals International Madurai IN
03 1ZHEJIANG CHANGMING PHARMACEUTICAL CO., LTD. Tiantai CN
01 3Tolbutamide
01 1China
02 2India
01 1Expired
02 2Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 2000-021 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-08-29
Type : Chemical
Substance Number : 304
Certificate Number : R0-CEP 2003-006 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2006-03-10
Type : Chemical
Substance Number : 304
Certificate Number : R0-CEP 2014-005 - Rev 00
Status : Expired
Issue Date : 2015-05-19
Type : Chemical
Substance Number : 304
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PharmaCompass offers a list of Tolbutamide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tolbutamide manufacturer or Tolbutamide supplier for your needs.
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A Restinon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Restinon, including repackagers and relabelers. The FDA regulates Restinon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Restinon 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 Restinon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Restinon supplier is an individual or a company that provides Restinon active pharmaceutical ingredient (API) or Restinon finished formulations upon request. The Restinon suppliers may include Restinon API manufacturers, exporters, distributors and traders.
click here to find a list of Restinon suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Restinon CEP of the European Pharmacopoeia monograph is often referred to as a Restinon Certificate of Suitability (COS). The purpose of a Restinon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Restinon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Restinon to their clients by showing that a Restinon CEP has been issued for it. The manufacturer submits a Restinon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Restinon CEP holder for the record. Additionally, the data presented in the Restinon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Restinon DMF.
A Restinon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Restinon 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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