01 1M/s. Kreative Organics Pvt. Ltd.
01 1Methenamine Hippurate USP
01 1WC-0180
01 1India
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 also assists you with knowing the Methenamine Hippurate API Price utilized in the formulation of products. Methenamine Hippurate API Price is not always fixed or binding as the Methenamine Hippurate Price is obtained through a variety of data sources. The Methenamine Hippurate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hexamethylenetetramine monohippurate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexamethylenetetramine monohippurate, including repackagers and relabelers. The FDA regulates Hexamethylenetetramine monohippurate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexamethylenetetramine monohippurate 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 Hexamethylenetetramine monohippurate supplier is an individual or a company that provides Hexamethylenetetramine monohippurate active pharmaceutical ingredient (API) or Hexamethylenetetramine monohippurate finished formulations upon request. The Hexamethylenetetramine monohippurate suppliers may include Hexamethylenetetramine monohippurate API manufacturers, exporters, distributors and traders.
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A Hexamethylenetetramine monohippurate written confirmation (Hexamethylenetetramine monohippurate WC) is an official document issued by a regulatory agency to a Hexamethylenetetramine monohippurate manufacturer, verifying that the manufacturing facility of a Hexamethylenetetramine monohippurate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hexamethylenetetramine monohippurate APIs or Hexamethylenetetramine monohippurate finished pharmaceutical products to another nation, regulatory agencies frequently require a Hexamethylenetetramine monohippurate WC (written confirmation) as part of the regulatory process.
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