01 1M/s Hetero Labs Ltd
02 1M/s Natco Pharma Ltd
03 1M/sMSN laboratories Pvt Lt
04 1M/sSionc Pharmaceuticals Pvt ltd
01 1Trifluridine IH
02 1Trifluridine IH/USP
03 1Trifluridine IP/USP
04 1Trifluridine USP
01 1WC-0041
02 1WC-0273
03 1WC-0349
04 1WC-0372n
01 4India
Date of Issue : 2022-07-16
Valid Till : 2025-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Sy. No. 10, I.D.A, Gaddapotharam (V), Jinnaram (M), Sangareddy District,...
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : Unit-II, Sy. No. 50, Kardanur (Village), Patancheru (Mandai), Sangareddy Distric...
Date of Issue : 2022-09-16
Valid Till : 2025-06-12
Written Confirmation Number : WC-0372n
Address of the Firm : S.No.73/1A, 74/7B, 78/1 B, 79/1, 2B, 3, 4B, 5, 6A, 6B, 7, 80/1, 2, 3, 4, 84/1, 2...
Date of Issue : 2023-11-15
Valid Till : 2026-05-11
Written Confirmation Number : WC-0273
Address of the Firm : Plot No: 34A, Road No: 1, Jawaharlal Nehru Pharma City, Thanam Village, Parawada...
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PharmaCompass offers a list of Trifluridine 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 Trifluridine manufacturer or Trifluridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trifluridine manufacturer or Trifluridine supplier.
PharmaCompass also assists you with knowing the Trifluridine API Price utilized in the formulation of products. Trifluridine API Price is not always fixed or binding as the Trifluridine Price is obtained through a variety of data sources. The Trifluridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Virophta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Virophta, including repackagers and relabelers. The FDA regulates Virophta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Virophta 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 Virophta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Virophta supplier is an individual or a company that provides Virophta active pharmaceutical ingredient (API) or Virophta finished formulations upon request. The Virophta suppliers may include Virophta API manufacturers, exporters, distributors and traders.
click here to find a list of Virophta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Virophta written confirmation (Virophta WC) is an official document issued by a regulatory agency to a Virophta manufacturer, verifying that the manufacturing facility of a Virophta active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Virophta APIs or Virophta finished pharmaceutical products to another nation, regulatory agencies frequently require a Virophta WC (written confirmation) as part of the regulatory process.
click here to find a list of Virophta suppliers with Written Confirmation (WC) on PharmaCompass.
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