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Status : Withdrawn by Holder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