DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddys Laboratories Ltd
02 1M/s Apitoria Pharma Limited
03 1M/s Chromo laboratories India Pvt ltd
04 2M/s Divi's Laboratories Limited
05 2M/s MSN Pharmachem Private Limited
06 1M/s Mylan laboratories Limited
07 2M/s Natco Pharma Limited
08 1M/s Nosch Labs Pvt Ltd
09 2M/s SMS Pharmaceuticals Limited
10 1M/s Sun Pharmaceuticals Industries ltd
11 1M/s Synergene Active Ingredients Pvt Ltd
12 1M/sLaxaiLifeSciencesPrivateLimited
13 1M/sTherapiva Pvt Ltd
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Sumatriptan Succinate Ph.Eur./USP
Date of Issue : 2022-05-27
Valid Till : 2025-06-04
Written Confirmation Number : WC-0043
Address of the Firm : Chemical Technical Operations ? Unit V, Peddadevulapally Village, Tripuraram Man...
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PharmaCompass offers a list of Sumatriptan 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 Sumatriptan manufacturer or Sumatriptan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sumatriptan manufacturer or Sumatriptan supplier.
PharmaCompass also assists you with knowing the Sumatriptan API Price utilized in the formulation of products. Sumatriptan API Price is not always fixed or binding as the Sumatriptan Price is obtained through a variety of data sources. The Sumatriptan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Frimig manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Frimig, including repackagers and relabelers. The FDA regulates Frimig manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Frimig 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 Frimig manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Frimig supplier is an individual or a company that provides Frimig active pharmaceutical ingredient (API) or Frimig finished formulations upon request. The Frimig suppliers may include Frimig API manufacturers, exporters, distributors and traders.
click here to find a list of Frimig suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Frimig written confirmation (Frimig WC) is an official document issued by a regulatory agency to a Frimig manufacturer, verifying that the manufacturing facility of a Frimig active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Frimig APIs or Frimig finished pharmaceutical products to another nation, regulatory agencies frequently require a Frimig WC (written confirmation) as part of the regulatory process.
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