Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Ipca Laboratories Limited
03 1SperaNexus Inc.
01 3Metoprolol tartrate
01 1India
02 1Japan
03 1Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 222MF10104
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2010-03-18
Latest Date of Registration : 2019-03-11
Registration Number : 221MF10151
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, INDIA
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2009-07-09
Registration Number : 217MF10047
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2008-01-10
A Metoprolol Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoprolol Tartrate, including repackagers and relabelers. The FDA regulates Metoprolol Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoprolol Tartrate 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 Metoprolol Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoprolol Tartrate supplier is an individual or a company that provides Metoprolol Tartrate active pharmaceutical ingredient (API) or Metoprolol Tartrate finished formulations upon request. The Metoprolol Tartrate suppliers may include Metoprolol Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Metoprolol Tartrate 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 Metoprolol Tartrate Drug Master File in Japan (Metoprolol Tartrate JDMF) empowers Metoprolol Tartrate 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 Metoprolol Tartrate JDMF during the approval evaluation for pharmaceutical products. At the time of Metoprolol Tartrate 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 Metoprolol Tartrate suppliers with JDMF on PharmaCompass.
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