01 1M/s Apothecon Pharmaceuticals Pvt. Ltd
01 1Benztropine Mesylate USP
01 1WC-0369
01 1India
Date of Issue : 2026-03-16
Valid Till : 2029-03-16
Written Confirmation Number : WC-0369
Address of the Firm : Plot No. 1134, 1135, 1136, 1137,1143B, 1144 A&B, 1138 A&B, Padra -Jambusar Highw...
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PharmaCompass offers a list of Benztropine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Benztropine manufacturer or Benztropine supplier for your needs.
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PharmaCompass also assists you with knowing the Benztropine API Price utilized in the formulation of products. Benztropine API Price is not always fixed or binding as the Benztropine Price is obtained through a variety of data sources. The Benztropine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MK 02 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK 02, including repackagers and relabelers. The FDA regulates MK 02 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK 02 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 MK 02 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MK 02 supplier is an individual or a company that provides MK 02 active pharmaceutical ingredient (API) or MK 02 finished formulations upon request. The MK 02 suppliers may include MK 02 API manufacturers, exporters, distributors and traders.
click here to find a list of MK 02 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MK 02 written confirmation (MK 02 WC) is an official document issued by a regulatory agency to a MK 02 manufacturer, verifying that the manufacturing facility of a MK 02 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MK 02 APIs or MK 02 finished pharmaceutical products to another nation, regulatory agencies frequently require a MK 02 WC (written confirmation) as part of the regulatory process.
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