01 1Assia Chemical Industries Ltd.
02 1Cambrex Profarmaco Milano S. r. l.
03 1Daiwa Pharmaceutical Industries Co., Ltd.
04 2Hetero Labs Limited
05 1Polaris AI Pharma Corp.
06 1Sanyo Chemical Research Institute Co., Ltd.
07 1Topharman Shandong Co. ,Ltd
08 1Valdepharm
09 1Yoshindo Co., Ltd.
01 4Aripiprazole
02 2Aripiprazole
03 1Aripiprazole "Teva"
04 1Aripiprazole (production only)
05 1Purification aripiprazole
06 1Sterile aripiprazole hydrate
01 1China
02 2Gabon
03 2India
04 1Israel
05 2Japan
06 1South Korea
07 1U.S.A
Registration Number : 228MF10057
Registrant's Address : Neot-Hovav Eco-Industrial Park, Be'er Sheva 8412316, Israel
Initial Date of Registration : 2016-02-18
Latest Date of Registration : 2016-02-18
Registration Number : 227MF10233
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2015-09-24
Latest Date of Registration : 2016-02-24
Registration Number : 228MF10024
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2016-02-02
Latest Date of Registration : 2016-02-02
Registration Number : 228MF10005
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2016-01-08
Latest Date of Registration : 2016-01-08
Registration Number : 306MF10017
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2024-01-24
Latest Date of Registration : 2024-01-24
Aripiprazole (for manufacturing purposes only)
Registration Number : 228MF10021
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2016-01-26
Latest Date of Registration : 2016-01-26
Aripiprazole "For manufacturing purposes only"
Registration Number : 303MF10143
Registrant's Address : 49 Wenshuibeilu, Xin'an District, Anqiu City, Weifang City, Shandong Province, China
Initial Date of Registration : 2021-09-02
Latest Date of Registration : 2021-09-02
Registration Number : 301MF10077
Registrant's Address : Parc Industriel d'Incarville Parc de la Fringale CS 10606 27106 Val de Reuil Cedex Fr...
Initial Date of Registration : 2019-10-18
Latest Date of Registration : 2019-10-18
Registration Number : 228MF10032
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2016-02-02
Latest Date of Registration : 2016-02-02
Registration Number : 227MF10286
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2015-12-15
Latest Date of Registration : 2016-11-22
A Abilify manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Abilify, including repackagers and relabelers. The FDA regulates Abilify manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Abilify 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 Abilify manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Abilify supplier is an individual or a company that provides Abilify active pharmaceutical ingredient (API) or Abilify finished formulations upon request. The Abilify suppliers may include Abilify API manufacturers, exporters, distributors and traders.
click here to find a list of Abilify 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 Abilify Drug Master File in Japan (Abilify JDMF) empowers Abilify 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 Abilify JDMF during the approval evaluation for pharmaceutical products. At the time of Abilify 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 Abilify suppliers with JDMF on PharmaCompass.
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