Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1M/s. Granules India Ltd
02 1M/s. Granules India Ltd.
03 1M/s Synthokem Labs Pvt ltd
04 1M/s. Synthochem Labs Pvt. Ltd.,
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-0028
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.
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0116
Address of the Firm : H. No. 6-5 & 6-11, Temple Road, Bonthapalli, Jinnaram Mandal, Medak Dist., Hyder...
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, Patanche...
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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 Bronkaid Caplets manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bronkaid Caplets, including repackagers and relabelers. The FDA regulates Bronkaid Caplets manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bronkaid Caplets 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 Bronkaid Caplets supplier is an individual or a company that provides Bronkaid Caplets active pharmaceutical ingredient (API) or Bronkaid Caplets finished formulations upon request. The Bronkaid Caplets suppliers may include Bronkaid Caplets API manufacturers, exporters, distributors and traders.
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A Bronkaid Caplets written confirmation (Bronkaid Caplets WC) is an official document issued by a regulatory agency to a Bronkaid Caplets manufacturer, verifying that the manufacturing facility of a Bronkaid Caplets active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bronkaid Caplets APIs or Bronkaid Caplets finished pharmaceutical products to another nation, regulatory agencies frequently require a Bronkaid Caplets WC (written confirmation) as part of the regulatory process.
click here to find a list of Bronkaid Caplets suppliers with Written Confirmation (WC) on PharmaCompass.
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