Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
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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
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01 7Guaifenesin
02 1Guaifenesin, BPL site
03 1Guaifenesin, Regular, milled
04 1Guaifenesin, Unit-II
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01 1China
02 1France
03 1Germany
04 6India
05 1Taiwan
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01 1Expired
02 8Valid
03 1Withdrawn by Holder
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
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
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.
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
Certificate Number : CEP 2019-065 - Rev 01
Status : Valid
Issue Date : 2025-01-15
Type : Chemical
Substance Number : 615
Certificate Number : R1-CEP 2002-194 - Rev 03
Status : Valid
Issue Date : 2018-06-22
Type : Chemical
Substance Number : 615
Certificate Number : R1-CEP 2009-351 - Rev 02
Status : Valid
Issue Date : 2020-06-18
Type : Chemical
Substance Number : 615
Certificate Number : R2-CEP 1994-008 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2006-08-31
Type : Chemical
Substance Number : 615
Certificate Number : R1-CEP 2008-275 - Rev 04
Status : Valid
Issue Date : 2021-04-09
Type : Chemical
Substance Number : 615
Certificate Number : CEP 2024-189 - Rev 00
Status : Valid
Issue Date : 2024-11-20
Type : Chemical
Substance Number : 615
Certificate Number : R0-CEP 2002-223 - Rev 01
Status : Expired
Issue Date : 2004-11-22
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guaifenesin manufacturer or Guaifenesin supplier.
PharmaCompass also assists you with knowing the Guaifenesin API Price utilized in the formulation of products. Guaifenesin API Price is not always fixed or binding as the Guaifenesin Price is obtained through a variety of data sources. The Guaifenesin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Guaifenesinum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Guaifenesinum, including repackagers and relabelers. The FDA regulates Guaifenesinum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Guaifenesinum 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 Guaifenesinum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Guaifenesinum supplier is an individual or a company that provides Guaifenesinum active pharmaceutical ingredient (API) or Guaifenesinum finished formulations upon request. The Guaifenesinum suppliers may include Guaifenesinum API manufacturers, exporters, distributors and traders.
click here to find a list of Guaifenesinum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Guaifenesinum CEP of the European Pharmacopoeia monograph is often referred to as a Guaifenesinum Certificate of Suitability (COS). The purpose of a Guaifenesinum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Guaifenesinum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Guaifenesinum to their clients by showing that a Guaifenesinum CEP has been issued for it. The manufacturer submits a Guaifenesinum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Guaifenesinum CEP holder for the record. Additionally, the data presented in the Guaifenesinum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Guaifenesinum DMF.
A Guaifenesinum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Guaifenesinum 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 Guaifenesinum suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Guaifenesinum
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