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01 1M/s Harman Finochem limited
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01 1Oxybutynin Chloride USP
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01 1WC-0045nA2
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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 Driptane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Driptane, including repackagers and relabelers. The FDA regulates Driptane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Driptane 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 Driptane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Driptane supplier is an individual or a company that provides Driptane active pharmaceutical ingredient (API) or Driptane finished formulations upon request. The Driptane suppliers may include Driptane API manufacturers, exporters, distributors and traders.
click here to find a list of Driptane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Driptane written confirmation (Driptane WC) is an official document issued by a regulatory agency to a Driptane manufacturer, verifying that the manufacturing facility of a Driptane active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Driptane APIs or Driptane finished pharmaceutical products to another nation, regulatory agencies frequently require a Driptane WC (written confirmation) as part of the regulatory process.
click here to find a list of Driptane suppliers with Written Confirmation (WC) on PharmaCompass.
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