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01 1M/sSurajlok Chemicals Pvt. Ltds
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01 1Procarbazine Hydrochloride USP
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01 1WC-0435
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01 1India
Procarbazine Hydrochloride USP
Date of Issue : 2022-12-09
Valid Till : 2025-01-20
Written Confirmation Number : WC-0435
Address of the Firm : Plot No. T-6, M.I.D.C, Tarapur Industrial Area, Boisar, Dist-Thane -401506 Mahar...
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PharmaCompass also assists you with knowing the Procarbazine Hydrochloride API Price utilized in the formulation of products. Procarbazine Hydrochloride API Price is not always fixed or binding as the Procarbazine Hydrochloride Price is obtained through a variety of data sources. The Procarbazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Natulan hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natulan hydrochloride, including repackagers and relabelers. The FDA regulates Natulan hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natulan 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.
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A Natulan hydrochloride supplier is an individual or a company that provides Natulan hydrochloride active pharmaceutical ingredient (API) or Natulan hydrochloride finished formulations upon request. The Natulan hydrochloride suppliers may include Natulan hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Natulan hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Natulan hydrochloride written confirmation (Natulan hydrochloride WC) is an official document issued by a regulatory agency to a Natulan hydrochloride manufacturer, verifying that the manufacturing facility of a Natulan hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Natulan hydrochloride APIs or Natulan hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Natulan hydrochloride WC (written confirmation) as part of the regulatory process.
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