01 2M/s Symed Labs Limited
01 1Phentermine Base IH
02 1Phentermine Hydrochloride USP
01 2WC-0072
01 2India
Date of Issue : 2022-11-28
Valid Till : 2025-09-08
Written Confirmation Number : WC-0072
Address of the Firm : Unit-ll, Plot No.: 25/B, Phase-lll, IDA, Jeedimetla (V), Quthbullapur (M), Medch...
Date of Issue : 2022-11-28
Valid Till : 2025-09-08
Written Confirmation Number : WC-0072
Address of the Firm : Unit-ll, Plot No.: 25/B, Phase-lll, IDA, Jeedimetla (V), Quthbullapur (M), Medch...
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A Ionamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ionamin, including repackagers and relabelers. The FDA regulates Ionamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ionamin 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 Ionamin supplier is an individual or a company that provides Ionamin active pharmaceutical ingredient (API) or Ionamin finished formulations upon request. The Ionamin suppliers may include Ionamin API manufacturers, exporters, distributors and traders.
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A Ionamin written confirmation (Ionamin WC) is an official document issued by a regulatory agency to a Ionamin manufacturer, verifying that the manufacturing facility of a Ionamin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ionamin APIs or Ionamin finished pharmaceutical products to another nation, regulatory agencies frequently require a Ionamin WC (written confirmation) as part of the regulatory process.
click here to find a list of Ionamin suppliers with Written Confirmation (WC) on PharmaCompass.
