01 1Active Pharma Co., Ltd.
02 1Aurobindo Pharma Limited
03 1DNP Fine Chemical Utsunomiya Co., Ltd.
04 1Daito Co., Ltd.
05 1Eli Lilly Kinsale Limited
06 1HETERO DRUGS LIMITED.
07 1JUBILANT BIOSYS LIMITED.
08 1JW Pharmaceutical Corporation
09 1Jiangsu Hansoh Pharmaceutical Group Co. , Ltd.
10 1Permachem Asia Co., Ltd.
11 1Shiratori Pharmaceutical Co., Ltd.
12 1Tateyama Chemical Co., Ltd.
13 2Tokuyama Corporation
14 1Yoshindo Co., Ltd.
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PharmaCompass offers a list of Olanzapine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Olanzapine manufacturer or Olanzapine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Olanzapine manufacturer or Olanzapine supplier.
A Apsico manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apsico, including repackagers and relabelers. The FDA regulates Apsico manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apsico 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 Apsico manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Apsico supplier is an individual or a company that provides Apsico active pharmaceutical ingredient (API) or Apsico finished formulations upon request. The Apsico suppliers may include Apsico API manufacturers, exporters, distributors and traders.
click here to find a list of Apsico suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Apsico Drug Master File in Japan (Apsico JDMF) empowers Apsico 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 Apsico JDMF during the approval evaluation for pharmaceutical products. At the time of Apsico 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 Apsico suppliers with JDMF on PharmaCompass.
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