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 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mepivacaine, including repackagers and relabelers. The FDA regulates Mepivacaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mepivacaine 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mepivacaine supplier is an individual or a company that provides Mepivacaine active pharmaceutical ingredient (API) or Mepivacaine finished formulations upon request. The Mepivacaine suppliers may include Mepivacaine API manufacturers, exporters, distributors and traders.
click here to find a list of Mepivacaine 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 Drug Master File in Japan (Mepivacaine JDMF) empowers Mepivacaine 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Mepivacaine 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 suppliers with JDMF on PharmaCompass.
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