01 1M/s. Sun Pharmaceuticals Industries Ltd.
02 1M/s. Symed Labs Limited
01 1Phentermine Hydrochloride USP/Phentermine Base IH
02 1Phentermine Hydrochloride(USP)
01 1WC-0072
02 1WC-0159
01 2India
Phentermine Hydrochloride(USP)
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm : A-7/A-8, MIDC, Ahmednagar-414 111, Maharashtra State
Phentermine Hydrochloride USP/Phentermine Base IH
Date of Issue : 2019-10-07
Valid Till : 2022-09-08
Written Confirmation Number : WC-0072
Address of the Firm : Plot No. 25/B, Phase-III, I.D.A., Jeedimetla, Hyderabad-500 055. AP.
A Ionamin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ionamin Hydrochloride, including repackagers and relabelers. The FDA regulates Ionamin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ionamin 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 Ionamin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ionamin Hydrochloride supplier is an individual or a company that provides Ionamin Hydrochloride active pharmaceutical ingredient (API) or Ionamin Hydrochloride finished formulations upon request. The Ionamin Hydrochloride suppliers may include Ionamin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ionamin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ionamin Hydrochloride written confirmation (Ionamin Hydrochloride WC) is an official document issued by a regulatory agency to a Ionamin Hydrochloride manufacturer, verifying that the manufacturing facility of a Ionamin Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ionamin Hydrochloride APIs or Ionamin Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Ionamin Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Ionamin Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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