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 Lonamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lonamin, including repackagers and relabelers. The FDA regulates Lonamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lonamin 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 Lonamin supplier is an individual or a company that provides Lonamin active pharmaceutical ingredient (API) or Lonamin finished formulations upon request. The Lonamin suppliers may include Lonamin API manufacturers, exporters, distributors and traders.
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A Lonamin written confirmation (Lonamin WC) is an official document issued by a regulatory agency to a Lonamin manufacturer, verifying that the manufacturing facility of a Lonamin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lonamin APIs or Lonamin finished pharmaceutical products to another nation, regulatory agencies frequently require a Lonamin WC (written confirmation) as part of the regulatory process.
click here to find a list of Lonamin suppliers with Written Confirmation (WC) on PharmaCompass.
