Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Cambrex Karlskoga AB
03 1SperaNexus Inc.
01 1LIDOCAINE HYDROCHLORIDE
02 2Lidocaine hydrochloride
01 1Japan
02 1Spain
03 1U.S.A
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 219MF10205
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2007-06-13
Latest Date of Registration : 2021-04-02
Registration Number : 218MF10963
Registrant's Address : SE-691 85 Karlskoga, SWEDEN
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2006-12-01
Registration Number : 217MF10050
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2009-01-28
A Lidocaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lidocaine Hydrochloride, including repackagers and relabelers. The FDA regulates Lidocaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lidocaine 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 Lidocaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lidocaine Hydrochloride supplier is an individual or a company that provides Lidocaine Hydrochloride active pharmaceutical ingredient (API) or Lidocaine Hydrochloride finished formulations upon request. The Lidocaine Hydrochloride suppliers may include Lidocaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Lidocaine 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 Lidocaine Hydrochloride Drug Master File in Japan (Lidocaine Hydrochloride JDMF) empowers Lidocaine 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 Lidocaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Lidocaine 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 Lidocaine Hydrochloride suppliers with JDMF on PharmaCompass.
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