Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1M/s. Rusan Pharma Limited
01 1Eflornithine Hydrochloride Monohydrate IH
01 1WC-0278
01 1India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Eflornithine Hydrochloride Monohydrate IH
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
A Eflornithine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eflornithine Hydrochloride, including repackagers and relabelers. The FDA regulates Eflornithine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eflornithine Hydrochloride 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 Eflornithine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eflornithine Hydrochloride supplier is an individual or a company that provides Eflornithine Hydrochloride active pharmaceutical ingredient (API) or Eflornithine Hydrochloride finished formulations upon request. The Eflornithine Hydrochloride suppliers may include Eflornithine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Eflornithine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eflornithine Hydrochloride written confirmation (Eflornithine Hydrochloride WC) is an official document issued by a regulatory agency to a Eflornithine Hydrochloride manufacturer, verifying that the manufacturing facility of a Eflornithine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eflornithine Hydrochloride APIs or Eflornithine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Eflornithine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Eflornithine Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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