01 1M/sSionc Pharmaceuticals Pvt ltd
01 1Nilutamide Ph.Eur
01 1WC-0273
01 1India
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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A Anandron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anandron, including repackagers and relabelers. The FDA regulates Anandron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anandron 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 Anandron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Anandron supplier is an individual or a company that provides Anandron active pharmaceutical ingredient (API) or Anandron finished formulations upon request. The Anandron suppliers may include Anandron API manufacturers, exporters, distributors and traders.
click here to find a list of Anandron suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Anandron written confirmation (Anandron WC) is an official document issued by a regulatory agency to a Anandron manufacturer, verifying that the manufacturing facility of a Anandron active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Anandron APIs or Anandron finished pharmaceutical products to another nation, regulatory agencies frequently require a Anandron WC (written confirmation) as part of the regulatory process.
click here to find a list of Anandron suppliers with Written Confirmation (WC) on PharmaCompass.
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