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 : R1-CEP 1999-088 - Rev 05
Status : Valid
Issue Date : 2018-06-26
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 : CEP 2019-065 - Rev 01
Status : Valid
Issue Date : 2025-01-15
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 Nasatab LA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nasatab LA, including repackagers and relabelers. The FDA regulates Nasatab LA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nasatab LA 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 Nasatab LA supplier is an individual or a company that provides Nasatab LA active pharmaceutical ingredient (API) or Nasatab LA finished formulations upon request. The Nasatab LA suppliers may include Nasatab LA API manufacturers, exporters, distributors and traders.
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A Nasatab LA CEP of the European Pharmacopoeia monograph is often referred to as a Nasatab LA Certificate of Suitability (COS). The purpose of a Nasatab LA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nasatab LA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nasatab LA to their clients by showing that a Nasatab LA CEP has been issued for it. The manufacturer submits a Nasatab LA CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nasatab LA CEP holder for the record. Additionally, the data presented in the Nasatab LA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nasatab LA DMF.
A Nasatab LA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nasatab LA 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 Nasatab LA suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Nasatab LA
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