01 1M/s Kreative Actives Private limited
02 1M/s. Apitoria Pharma Private Limited
03 1M/sKreative Organics Private limited
01 1Methenamine Hippurate IH
02 2Methenamine Hippurate USP
01 1WC-0023
02 1WC-0180
03 1WC-0599
01 3India
Date of Issue : 2025-07-11
Valid Till : 2028-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy. No\'s. 52,53,58,59,61 to 78, 127 & 128, Pydibhimavaram Village & Sy. No\'s. ...
Date of Issue : 2024-12-20
Valid Till : 2027-12-19
Written Confirmation Number : WC-0599
Address of the Firm : Plot No. 15B6, APSEZ, De- Notified Area, Atchutapuram, Krishnampalem (V), Rambil...
Date of Issue : 2022-08-29
Valid Till : 2025-07-26
Written Confirmation Number : WC-0180
Address of the Firm : D-123, Phase -III, IDA., Jeedimetla (V), Quthbullapur (M), Medchal-Malkajgiri Di...
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PharmaCompass offers a list of Methenamine Hippurate 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 Methenamine Hippurate manufacturer or Methenamine Hippurate supplier for your needs.
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A hexamine hippurate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of hexamine hippurate, including repackagers and relabelers. The FDA regulates hexamine hippurate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. hexamine hippurate 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 hexamine hippurate supplier is an individual or a company that provides hexamine hippurate active pharmaceutical ingredient (API) or hexamine hippurate finished formulations upon request. The hexamine hippurate suppliers may include hexamine hippurate API manufacturers, exporters, distributors and traders.
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A hexamine hippurate written confirmation (hexamine hippurate WC) is an official document issued by a regulatory agency to a hexamine hippurate manufacturer, verifying that the manufacturing facility of a hexamine hippurate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting hexamine hippurate APIs or hexamine hippurate finished pharmaceutical products to another nation, regulatory agencies frequently require a hexamine hippurate WC (written confirmation) as part of the regulatory process.
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