01 1M/s. Aurobindo Pharma Ltd.,
01 1Ribavirin (EP)
01 1WC-0120
01 1India
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0120
Address of the Firm : Unit-1, Sy. No. 388 & 389, Borpatla (V), Hatnoora (M), Medak (Dist).502 296 A.P....
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A Vilona manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vilona, including repackagers and relabelers. The FDA regulates Vilona manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vilona 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 Vilona manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vilona supplier is an individual or a company that provides Vilona active pharmaceutical ingredient (API) or Vilona finished formulations upon request. The Vilona suppliers may include Vilona API manufacturers, exporters, distributors and traders.
click here to find a list of Vilona suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vilona written confirmation (Vilona WC) is an official document issued by a regulatory agency to a Vilona manufacturer, verifying that the manufacturing facility of a Vilona active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vilona APIs or Vilona finished pharmaceutical products to another nation, regulatory agencies frequently require a Vilona WC (written confirmation) as part of the regulatory process.
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