01 1M/s Sionc Phamaceuticals Pvt Ltd
01 1Chlorambucil IH/EP
01 1WC-0273
01 1India
Date of Issue : 2020-07-23
Valid Till : 2023-05-11
Written Confirmation Number : WC-0273
Address of the Firm : Plot No. 34A, J.N.Pharma City, Thanam (V), Parawada (M), Vishakhapatnam-District...
A Leukeran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Leukeran, including repackagers and relabelers. The FDA regulates Leukeran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Leukeran 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 Leukeran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Leukeran supplier is an individual or a company that provides Leukeran active pharmaceutical ingredient (API) or Leukeran finished formulations upon request. The Leukeran suppliers may include Leukeran API manufacturers, exporters, distributors and traders.
click here to find a list of Leukeran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Leukeran written confirmation (Leukeran WC) is an official document issued by a regulatory agency to a Leukeran manufacturer, verifying that the manufacturing facility of a Leukeran active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Leukeran APIs or Leukeran finished pharmaceutical products to another nation, regulatory agencies frequently require a Leukeran WC (written confirmation) as part of the regulatory process.
click here to find a list of Leukeran suppliers with Written Confirmation (WC) on PharmaCompass.
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