Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1M/s Rusan Pharma Ltd
02 1M/s Sun Pharmaceuticals Industries ltd
01 1Naltrexone Hydrochloride EP/USP
02 1Naltrexone Hydrochloride USP/Ph.Eur.
01 1WC-0168
02 1WC-0278
01 2India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Naltrexone Hydrochloride EP/USP
Date of Issue : 2025-02-11
Valid Till : 2027-06-09
Written Confirmation Number : WC-0278
Address of the Firm : Plot No.6406, 6407 & 6411, GIDC Estate, Ankleshwar-393002, Dist- Bharuch
Naltrexone Hydrochloride USP/Ph.Eur.
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.-...
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A Celupan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celupan, including repackagers and relabelers. The FDA regulates Celupan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celupan 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 Celupan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Celupan supplier is an individual or a company that provides Celupan active pharmaceutical ingredient (API) or Celupan finished formulations upon request. The Celupan suppliers may include Celupan API manufacturers, exporters, distributors and traders.
click here to find a list of Celupan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Celupan written confirmation (Celupan WC) is an official document issued by a regulatory agency to a Celupan manufacturer, verifying that the manufacturing facility of a Celupan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Celupan APIs or Celupan finished pharmaceutical products to another nation, regulatory agencies frequently require a Celupan WC (written confirmation) as part of the regulatory process.
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