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