Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Cambrex Karlskoga AB
03 1Delta Synthetic Co. , Ltd.
04 1SWATI SPENTOSE PRIVATE LIMITED
05 1SperaNexus Inc.
01 1Day stations lidocaine (production only)
02 4Lidocaine
01 1India
02 1Japan
03 1Spain
04 1Taiwan
05 1U.S.A
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 217MF11155
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2021-03-05
Registration Number : 222MF10045
Registrant's Address : SE-691 85 Karlskoga, SWEDEN
Initial Date of Registration : 2010-02-09
Latest Date of Registration : 2018-04-09
Japanese Pharmacopoeia Lidocaine (for manufacturing purposes only)
Registration Number : 218MF10093
Registrant's Address : 15, Minsheng St. , Tucheng Dist. , New Taipei City 23679, Taiwan (R.O.C.)
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2017-06-15
Registration Number : 217MF10032
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2006-06-09
Registration Number : 226MF10092
Registrant's Address : 114 Marine Chambers, 11, New Marine Lines, Mumbai-400 020, INDIA
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2014-05-14
A LIDODERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDODERM, including repackagers and relabelers. The FDA regulates LIDODERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDODERM 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 LIDODERM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIDODERM supplier is an individual or a company that provides LIDODERM active pharmaceutical ingredient (API) or LIDODERM finished formulations upon request. The LIDODERM suppliers may include LIDODERM API manufacturers, exporters, distributors and traders.
click here to find a list of LIDODERM 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 LIDODERM Drug Master File in Japan (LIDODERM JDMF) empowers LIDODERM 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 LIDODERM JDMF during the approval evaluation for pharmaceutical products. At the time of LIDODERM 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 LIDODERM suppliers with JDMF on PharmaCompass.
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