Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1Zhejiang Hengkang Pharmaceutical
02 1M/s. Aurore Life Sciences
01 1Favipiravir
02 1Favipiravir IH
01 1WC-0119A10
02 1ZJ210055
01 1China
02 1India
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Date of Issue : 2021-01-28
Valid Till : 2024-08-17
Written Confirmation Number : ZJ210055
Address of the Firm : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China 317100
Date of Issue : 2021-10-13
Valid Till : 2022-07-02
Written Confirmation Number : WC-0119A10
Address of the Firm : Plot No. 35, 36, 38, 39, 40, 49, 50, & 51, Phase IV, IDA, Jeedimetla, Medchal-Ma...
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PharmaCompass also assists you with knowing the Favipiravir API Price utilized in the formulation of products. Favipiravir API Price is not always fixed or binding as the Favipiravir Price is obtained through a variety of data sources. The Favipiravir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Favipiravir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Favipiravir, including repackagers and relabelers. The FDA regulates Favipiravir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Favipiravir 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 Favipiravir supplier is an individual or a company that provides Favipiravir active pharmaceutical ingredient (API) or Favipiravir finished formulations upon request. The Favipiravir suppliers may include Favipiravir API manufacturers, exporters, distributors and traders.
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A Favipiravir written confirmation (Favipiravir WC) is an official document issued by a regulatory agency to a Favipiravir manufacturer, verifying that the manufacturing facility of a Favipiravir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Favipiravir APIs or Favipiravir finished pharmaceutical products to another nation, regulatory agencies frequently require a Favipiravir WC (written confirmation) as part of the regulatory process.
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