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