01 1M/s S.M.S Pharmaceuticals Ltd
01 1Penciclovir IHS
01 1WC-0373
01 1India
Date of Issue : 2022-07-08
Valid Till : 2025-07-21
Written Confirmation Number : WC-0373
Address of the Firm : Unit-VII Kandivalasa (V) Poosapatirega (M) Vizianagaram District, Andhra Pradesh...
A Penciclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penciclovir, including repackagers and relabelers. The FDA regulates Penciclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penciclovir 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 Penciclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Penciclovir supplier is an individual or a company that provides Penciclovir active pharmaceutical ingredient (API) or Penciclovir finished formulations upon request. The Penciclovir suppliers may include Penciclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Penciclovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Penciclovir written confirmation (Penciclovir WC) is an official document issued by a regulatory agency to a Penciclovir manufacturer, verifying that the manufacturing facility of a Penciclovir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Penciclovir APIs or Penciclovir finished pharmaceutical products to another nation, regulatory agencies frequently require a Penciclovir WC (written confirmation) as part of the regulatory process.
click here to find a list of Penciclovir suppliers with Written Confirmation (WC) on PharmaCompass.
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