Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 2GRANULES INDIA LIMITED Hyderabad IN
02 2SYNTHOKEM LABS PRIVATE LIMITED Hyderabad IN
03 1BIESTERFELD SPEZIALCHEMIE GMBH Hamburg DE
04 1DELTA SYNTHETIC CO., LTD. New Taipei City TW
05 1M/s Stellar Chemical Laboratories PVT Limited Mumbai IN
06 1RHODIA OPERATIONS SAS Aubervilliers FR
07 1SEVEN STAR PHARMACEUTICAL COMPANY, LTD. New Taipei City TW
08 1SMILAX LABORATORIES LIMITED Hyderabad IN
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Certificate Number : R1-CEP 2009-201 - Rev 03
Status : Valid
Issue Date : 2018-11-27
Type : Chemical
Substance Number : 615
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
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Certificate Number : R0-CEP 2021-332 - Rev 00
Status : Valid
Issue Date : 2021-12-10
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Status : Withdrawn by Holder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
70
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 DSSTox_CID_3114 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3114, including repackagers and relabelers. The FDA regulates DSSTox_CID_3114 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3114 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 DSSTox_CID_3114 supplier is an individual or a company that provides DSSTox_CID_3114 active pharmaceutical ingredient (API) or DSSTox_CID_3114 finished formulations upon request. The DSSTox_CID_3114 suppliers may include DSSTox_CID_3114 API manufacturers, exporters, distributors and traders.
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A DSSTox_CID_3114 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_3114 Certificate of Suitability (COS). The purpose of a DSSTox_CID_3114 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_3114 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_3114 to their clients by showing that a DSSTox_CID_3114 CEP has been issued for it. The manufacturer submits a DSSTox_CID_3114 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_3114 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_3114 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_3114 DMF.
A DSSTox_CID_3114 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_3114 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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We have 8 companies offering DSSTox_CID_3114
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