Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
01 2SYNTHOKEM LABS PRIVATE LIMITED Hyderabad IN
02 1BIESTERFELD SPEZIALCHEMIE GMBH Hamburg DE
03 1DELTA SYNTHETIC CO., LTD. New Taipei City TW
04 1M/s Stellar Chemical Laboratories PVT Limited Mumbai IN
05 1RHODIA OPERATIONS SAS Aubervilliers FR
06 1SEVEN STAR PHARMACEUTICAL COMPANY, LTD. New Taipei City TW
07 1SMILAX LABORATORIES LIMITED Hyderabad IN
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
Certificate Number : CEP 2019-065 - Rev 01
Status : Valid
Issue Date : 2025-01-15
Type : Chemical
Substance Number : 615
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
Certificate Number : R1-CEP 1999-088 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2018-06-26
Type : Chemical
Substance Number : 615
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PharmaCompass offers a list of Guaifenesin 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 Guaifenesin manufacturer or Guaifenesin supplier for your needs.
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A Hustosil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hustosil, including repackagers and relabelers. The FDA regulates Hustosil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hustosil 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 Hustosil supplier is an individual or a company that provides Hustosil active pharmaceutical ingredient (API) or Hustosil finished formulations upon request. The Hustosil suppliers may include Hustosil API manufacturers, exporters, distributors and traders.
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A Hustosil CEP of the European Pharmacopoeia monograph is often referred to as a Hustosil Certificate of Suitability (COS). The purpose of a Hustosil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hustosil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hustosil to their clients by showing that a Hustosil CEP has been issued for it. The manufacturer submits a Hustosil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hustosil CEP holder for the record. Additionally, the data presented in the Hustosil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hustosil DMF.
A Hustosil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hustosil 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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