01 Amoli Organics (A Division of Umedica Laboratories Pvt Ltd.) (1)
02 Katsura Chemical Co., Ltd. (1)
03 Shizuoka Caffeine Industry Co., Ltd. (1)
04 Yamamoto Chemical Industry Co., Ltd. (2)
05 Zhejiang Jiuzhou Pharmaceutical Co. , Ltd. (1)
06 Zhejiang Raybow Pharmaceutical Co. , Ltd. (1)
01 Carbamazepine (3)
02 Carbamazepine (production only) (1)
03 Japanese Pharmacopoeia carbamazepine (2)
04 Japanese Pharmacopoeia carbamazepine (production only) (1)
01 China (1)
02 India (1)
03 Japan (4)
04 U.S.A (1)
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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 Tox21_300195 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300195, including repackagers and relabelers. The FDA regulates Tox21_300195 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300195 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_300195 supplier is an individual or a company that provides Tox21_300195 active pharmaceutical ingredient (API) or Tox21_300195 finished formulations upon request. The Tox21_300195 suppliers may include Tox21_300195 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300195 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 Tox21_300195 Drug Master File in Japan (Tox21_300195 JDMF) empowers Tox21_300195 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 Tox21_300195 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300195 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 6 companies offering Tox21_300195
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