01 1AMSA S. p. A.
01 1METOCLOPRAMIDE DIHYDROCHLORIDE
01 1Italy
METOCLOPRAMIDE DIHYDROCHLORIDE
Registration Number : 221MF10057
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2009-03-19
Latest Date of Registration : 2020-04-02
A Metoclopramide Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoclopramide Hydrochloride, including repackagers and relabelers. The FDA regulates Metoclopramide Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoclopramide 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 Metoclopramide Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoclopramide Hydrochloride supplier is an individual or a company that provides Metoclopramide Hydrochloride active pharmaceutical ingredient (API) or Metoclopramide Hydrochloride finished formulations upon request. The Metoclopramide Hydrochloride suppliers may include Metoclopramide Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Metoclopramide Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Metoclopramide Hydrochloride Drug Master File in Japan (Metoclopramide Hydrochloride JDMF) empowers Metoclopramide Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Metoclopramide Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Metoclopramide Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Metoclopramide Hydrochloride suppliers with JDMF on PharmaCompass.
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