01 1M/s. Concord Biotech Ltd.,
01 1Cyclosporine (USP/Ph. Eur.)
01 1WC-0111
01 1India
Date of Issue : 2019-09-23
Valid Till : 2022-07-02
Written Confirmation Number : WC-0111
Address of the Firm : Plot No. 1482-1486, Trasad Road, Dholka, Dist- Ahmedabad
A Restasis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Restasis, including repackagers and relabelers. The FDA regulates Restasis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Restasis 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 Restasis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Restasis supplier is an individual or a company that provides Restasis active pharmaceutical ingredient (API) or Restasis finished formulations upon request. The Restasis suppliers may include Restasis API manufacturers, exporters, distributors and traders.
click here to find a list of Restasis suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Restasis written confirmation (Restasis WC) is an official document issued by a regulatory agency to a Restasis manufacturer, verifying that the manufacturing facility of a Restasis active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Restasis APIs or Restasis finished pharmaceutical products to another nation, regulatory agencies frequently require a Restasis WC (written confirmation) as part of the regulatory process.
click here to find a list of Restasis suppliers with Written Confirmation (WC) on PharmaCompass.
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