Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1M/s. Rusan Pharma Limited
02 1M/s. Sun Pharmaceuticals Ltd.
01 1Naloxone HCl EP/BP/USP
02 1Naloxone Hydrochloride Dihydrate EP/USP
01 1WC-0168
02 1WC-0278
01 2India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Date of Issue : 2021-08-27
Valid Till : 2024-06-10
Written Confirmation Number : WC-0278
Address of the Firm : Plot No. 6406, GIDC Estate, Ankleshwar-393002, Dist. Bharuch, Gujarat
Naloxone Hydrochloride Dihydrate EP/USP
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC, Industrial Zone, At & Post - Panoli, Dist....
A Naloxone Hydrochloride Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naloxone Hydrochloride Dihydrate, including repackagers and relabelers. The FDA regulates Naloxone Hydrochloride Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate supplier is an individual or a company that provides Naloxone Hydrochloride Dihydrate active pharmaceutical ingredient (API) or Naloxone Hydrochloride Dihydrate finished formulations upon request. The Naloxone Hydrochloride Dihydrate suppliers may include Naloxone Hydrochloride Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Naloxone Hydrochloride Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Naloxone Hydrochloride Dihydrate written confirmation (Naloxone Hydrochloride Dihydrate WC) is an official document issued by a regulatory agency to a Naloxone Hydrochloride Dihydrate manufacturer, verifying that the manufacturing facility of a Naloxone Hydrochloride Dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Naloxone Hydrochloride Dihydrate APIs or Naloxone Hydrochloride Dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Naloxone Hydrochloride Dihydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Naloxone Hydrochloride Dihydrate suppliers with Written Confirmation (WC) on PharmaCompass.
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