01 1M/s. Apicore Pharmaceuticals Pvt. Ltd.,
02 1MSN Laboratories Pvt. Ltd.
01 1Ponatinib Hydrochloride IH
02 1Ponatinib Hydrochloride IHS
01 1WC-0110n
02 1WC-0349
01 2India
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0110n
Address of the Firm : 252-253, Dhobikuva-391 440, Opp.Jain Irrigation, Padra Jambusar Highway, Tal.Pad...
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
A Ponatinib Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ponatinib Hydrochloride, including repackagers and relabelers. The FDA regulates Ponatinib Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ponatinib Hydrochloride 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 Ponatinib Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ponatinib Hydrochloride supplier is an individual or a company that provides Ponatinib Hydrochloride active pharmaceutical ingredient (API) or Ponatinib Hydrochloride finished formulations upon request. The Ponatinib Hydrochloride suppliers may include Ponatinib Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ponatinib Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ponatinib Hydrochloride written confirmation (Ponatinib Hydrochloride WC) is an official document issued by a regulatory agency to a Ponatinib Hydrochloride manufacturer, verifying that the manufacturing facility of a Ponatinib Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ponatinib Hydrochloride APIs or Ponatinib Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Ponatinib Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Ponatinib Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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