Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Siegfried Evionnaz SA
01 1Hydrochloric acid mepivacaine
02 1MEPIVACAINE HYDROCHLORIDE
01 1Spain
02 1Switzerland
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 228MF10136
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2016-07-27
Latest Date of Registration : 2023-08-09
Registration Number : 218MF10524
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2024-08-28
A Mepivacaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mepivacaine Hydrochloride, including repackagers and relabelers. The FDA regulates Mepivacaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mepivacaine 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 Mepivacaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mepivacaine Hydrochloride supplier is an individual or a company that provides Mepivacaine Hydrochloride active pharmaceutical ingredient (API) or Mepivacaine Hydrochloride finished formulations upon request. The Mepivacaine Hydrochloride suppliers may include Mepivacaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Mepivacaine 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 Mepivacaine Hydrochloride Drug Master File in Japan (Mepivacaine Hydrochloride JDMF) empowers Mepivacaine 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 Mepivacaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Mepivacaine 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 Mepivacaine Hydrochloride suppliers with JDMF on PharmaCompass.
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