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 : 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 : R0-CEP 2019-065 - Rev 00
Status : Valid
Issue Date : 2019-11-27
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 : 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 : R1-CEP 1999-088 - Rev 05
Status : Valid
Issue Date : 2018-06-26
Type : Chemical
Substance Number : 615
A Guaifenesin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Guaifenesin, including repackagers and relabelers. The FDA regulates Guaifenesin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Guaifenesin 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 Guaifenesin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Guaifenesin supplier is an individual or a company that provides Guaifenesin active pharmaceutical ingredient (API) or Guaifenesin finished formulations upon request. The Guaifenesin suppliers may include Guaifenesin API manufacturers, exporters, distributors and traders.
click here to find a list of Guaifenesin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Guaifenesin CEP of the European Pharmacopoeia monograph is often referred to as a Guaifenesin Certificate of Suitability (COS). The purpose of a Guaifenesin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Guaifenesin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Guaifenesin to their clients by showing that a Guaifenesin CEP has been issued for it. The manufacturer submits a Guaifenesin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Guaifenesin CEP holder for the record. Additionally, the data presented in the Guaifenesin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Guaifenesin DMF.
A Guaifenesin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Guaifenesin 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 Guaifenesin suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Guaifenesin
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