01 1Amoli Organics (A Division of Umedica Laboratories Pvt Ltd.)
02 1Katsura Chemical Co., Ltd.
03 1Shizuoka Caffeine Industry Co., Ltd.
04 2Yamamoto Chemical Industry Co., Ltd.
05 1Zhejiang Jiuzhou Pharmaceutical Co. , Ltd.
06 1Zhejiang Raybow Pharmaceutical Co. , Ltd.
01 3Carbamazepine
02 1Carbamazepine (production only)
03 2Japanese Pharmacopoeia carbamazepine
04 1Japanese Pharmacopoeia carbamazepine (production only)
01 1China
02 1India
03 4Japan
04 1U.S.A
Registration Number : 230MF10157
Registrant's Address : 407, Dalamal House, Jamnalal Bajaj Road, Nariman Point, Mumbai-400021. India.
Initial Date of Registration : 2018-11-16
Latest Date of Registration : 2018-11-16
Registration Number : 218MF10271
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2006-02-17
Japanese Pharmacopoeia Carbamazepine (for manufacturing purposes only)
Registration Number : 226MF10090
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2014-05-09
Japanese Pharmacopoeia Carbamazepine
Registration Number : 226MF10214
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2014-11-17
Latest Date of Registration : 2014-11-17
Japanese Pharmacopoeia Carbamazepine
Registration Number : 220MF10261
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2008-12-22
Latest Date of Registration : 2008-12-22
Carbamazepine (for manufacturing purposes only)
Registration Number : 220MF10174
Registrant's Address : Waisha Road 99, Jiaojiang, Taizhou City, Zhejiang, China 318000
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2008-07-31
Registration Number : 230MF10068
Registrant's Address : 18 Nan Yang San Road, Lin Hai City, Taizhou City Zhejiang Province
Initial Date of Registration : 2018-05-31
Latest Date of Registration : 2024-09-11
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PharmaCompass offers a list of Carbamazepine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Carbamazepine manufacturer or Carbamazepine supplier for your needs.
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PharmaCompass also assists you with knowing the Carbamazepine API Price utilized in the formulation of products. Carbamazepine API Price is not always fixed or binding as the Carbamazepine Price is obtained through a variety of data sources. The Carbamazepine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Finlepsin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Finlepsin, including repackagers and relabelers. The FDA regulates Finlepsin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Finlepsin 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 Finlepsin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Finlepsin supplier is an individual or a company that provides Finlepsin active pharmaceutical ingredient (API) or Finlepsin finished formulations upon request. The Finlepsin suppliers may include Finlepsin API manufacturers, exporters, distributors and traders.
click here to find a list of Finlepsin 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 Finlepsin Drug Master File in Japan (Finlepsin JDMF) empowers Finlepsin 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 Finlepsin JDMF during the approval evaluation for pharmaceutical products. At the time of Finlepsin 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 Finlepsin suppliers with JDMF on PharmaCompass.
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