01 1M/s Harman Finochem limited
02 1M/s Resonance Laboratories Pvt ltd
03 1M/s Thinq Pharma CRO Limited
01 1Oxybutynin Hydrochloride BP/EP
02 1Oxybutynin Hydrochloride Ph. Eur
03 1Oxybutynin Hydrochloride/chloride USP/PH.Eur/BP
01 1WC-0045
02 1WC-0286
03 1WC-0585
01 3India
Oxybutynin Hydrochloride BP/EP
Date of Issue : 2025-11-12
Valid Till : 2028-11-11
Written Confirmation Number : WC-0045
Address of the Firm : Plot No. E-7, E-8, E-9, MIDC Industrial Area, Chikalthana, Aurangabad-431006 Mah...
Oxybutynin Hydrochloride Ph. Eur
Date of Issue : 2019-01-21
Valid Till : 2025-01-20
Written Confirmation Number : WC-0286
Address of the Firm : No. 8C & 9A, KIADB Industrial Area, Doddaballapur, Bangalore Dist. 561 023 Karna...
Oxybutynin Hydrochloride/chloride USP/PH.Eur/BP
Date of Issue : 2024-06-24
Valid Till : 2024-06-24
Written Confirmation Number : WC-0585
Address of the Firm : Plot No. m 40 and 42, sector 3, Pithampur Dhar MP India
26
PharmaCompass offers a list of Oxybutynin Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Oxybutynin Hydrochloride manufacturer or Oxybutynin Hydrochloride supplier for your needs.
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A Oxibutinina hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxibutinina hydrochloride, including repackagers and relabelers. The FDA regulates Oxibutinina hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxibutinina 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 Oxibutinina hydrochloride supplier is an individual or a company that provides Oxibutinina hydrochloride active pharmaceutical ingredient (API) or Oxibutinina hydrochloride finished formulations upon request. The Oxibutinina hydrochloride suppliers may include Oxibutinina hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxibutinina hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Oxibutinina hydrochloride written confirmation (Oxibutinina hydrochloride WC) is an official document issued by a regulatory agency to a Oxibutinina hydrochloride manufacturer, verifying that the manufacturing facility of a Oxibutinina hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxibutinina hydrochloride APIs or Oxibutinina hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxibutinina hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Oxibutinina hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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