01 1M/s Harman Finochem limited
01 1Oxybutynin Chloride USP
01 1WC-0045nA2
01 1India
Date of Issue : 2022-08-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm : Plot No. E-7, E-8, E-9, MIDC Industrial Area, Chikalthana, Aurangabad-431006
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PharmaCompass offers a list of Oxybutynin 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 Oxybutynin manufacturer or Oxybutynin supplier for your needs.
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PharmaCompass also assists you with knowing the Oxybutynin API Price utilized in the formulation of products. Oxybutynin API Price is not always fixed or binding as the Oxybutynin Price is obtained through a variety of data sources. The Oxybutynin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dresplan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dresplan, including repackagers and relabelers. The FDA regulates Dresplan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dresplan 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 Dresplan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dresplan supplier is an individual or a company that provides Dresplan active pharmaceutical ingredient (API) or Dresplan finished formulations upon request. The Dresplan suppliers may include Dresplan API manufacturers, exporters, distributors and traders.
click here to find a list of Dresplan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dresplan written confirmation (Dresplan WC) is an official document issued by a regulatory agency to a Dresplan manufacturer, verifying that the manufacturing facility of a Dresplan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dresplan APIs or Dresplan finished pharmaceutical products to another nation, regulatory agencies frequently require a Dresplan WC (written confirmation) as part of the regulatory process.
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