Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1M/s Granules India Limited
02 1M/s Granules India Ltd
03 1M/s Synthokem Labs Private Limited
04 1M/s Synthokem Labs Private Limited Unite-II
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0028n
Address of the Firm : 15A/1, IDA, Phase-III, Jeedimetla, Quthbullapur Mandai, Medchal-Malkajgiri Distr...
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0020n
Address of the Firm : B-5, Industrial Estate, Sanath Nagar, Hyderabad District -500018, Telangana, Ind...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Guaifenesin IH/BP/IP/USP/Ph. Eur
Date of Issue : 2022-06-29
Valid Till : 2025-02-07
Written Confirmation Number : WC-0116a1
Address of the Firm : Temple Road Bonthapally Bonthpally Village, Sangareddy-502313, Telangana India
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
Date of Issue : 2022-06-29
Valid Till : 2025-07-14
Written Confirmation Number : WC-0358
Address of the Firm : Unit-II, Plot No. 222 to 224 and 235 to 237, Phase -II, IDA, Pashamylaram, Pasha...
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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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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 component of Quibron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of Quibron, including repackagers and relabelers. The FDA regulates component of Quibron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of Quibron 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 component of Quibron supplier is an individual or a company that provides component of Quibron active pharmaceutical ingredient (API) or component of Quibron finished formulations upon request. The component of Quibron suppliers may include component of Quibron API manufacturers, exporters, distributors and traders.
click here to find a list of component of Quibron suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A component of Quibron written confirmation (component of Quibron WC) is an official document issued by a regulatory agency to a component of Quibron manufacturer, verifying that the manufacturing facility of a component of Quibron active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting component of Quibron APIs or component of Quibron finished pharmaceutical products to another nation, regulatory agencies frequently require a component of Quibron WC (written confirmation) as part of the regulatory process.
click here to find a list of component of Quibron suppliers with Written Confirmation (WC) on PharmaCompass.
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