Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 2M/s Rusan Pharma Ltd
01 1Apomorphine Hydrochloride USP
02 1Apomorphine Hydrochloride hemihydrate EP
01 2WC-0278
01 2India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Apomorphine Hydrochloride hemihydrate EP
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
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
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
31
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A Apomorphine hydrochloride hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apomorphine hydrochloride hydrate, including repackagers and relabelers. The FDA regulates Apomorphine hydrochloride hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apomorphine hydrochloride hydrate 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 Apomorphine hydrochloride hydrate supplier is an individual or a company that provides Apomorphine hydrochloride hydrate active pharmaceutical ingredient (API) or Apomorphine hydrochloride hydrate finished formulations upon request. The Apomorphine hydrochloride hydrate suppliers may include Apomorphine hydrochloride hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Apomorphine hydrochloride hydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Apomorphine hydrochloride hydrate written confirmation (Apomorphine hydrochloride hydrate WC) is an official document issued by a regulatory agency to a Apomorphine hydrochloride hydrate manufacturer, verifying that the manufacturing facility of a Apomorphine hydrochloride hydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Apomorphine hydrochloride hydrate APIs or Apomorphine hydrochloride hydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Apomorphine hydrochloride hydrate WC (written confirmation) as part of the regulatory process.
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