01 1Assia Chemical Industries Ltd.
02 1Cambrex Profarmaco Milano S. r. l.
03 1Daito Co., Ltd.
04 2Hetero Labs Limited
05 1Polaris AI Pharma Corp.
06 1Topharman Shandong Co. ,Ltd
07 1Yoshindo Co., Ltd.
01 3Aripiprazole
02 2Aripiprazole
03 1Aripiprazole "Teva"
04 1Aripiprazole (production only)
05 1Purification aripiprazole
01 1China
02 2India
03 1Israel
04 2Japan
05 1South Korea
06 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 : 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
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 : 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
Aripiprazole (for manufacturing purposes only)
Registration Number : 228MF10021
Registrant's Address : 326 Yokamachi, 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 : 227MF10286
Registrant's Address : 3697-8 Hagishima, Funamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2015-12-15
Latest Date of Registration : 2016-11-22
15
PharmaCompass offers a list of Aripiprazole 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 Aripiprazole manufacturer or Aripiprazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aripiprazole manufacturer or Aripiprazole supplier.
PharmaCompass also assists you with knowing the Aripiprazole API Price utilized in the formulation of products. Aripiprazole API Price is not always fixed or binding as the Aripiprazole Price is obtained through a variety of data sources. The Aripiprazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DL-178 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DL-178, including repackagers and relabelers. The FDA regulates DL-178 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DL-178 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 DL-178 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DL-178 supplier is an individual or a company that provides DL-178 active pharmaceutical ingredient (API) or DL-178 finished formulations upon request. The DL-178 suppliers may include DL-178 API manufacturers, exporters, distributors and traders.
click here to find a list of DL-178 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 DL-178 Drug Master File in Japan (DL-178 JDMF) empowers DL-178 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 DL-178 JDMF during the approval evaluation for pharmaceutical products. At the time of DL-178 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 DL-178 suppliers with JDMF on PharmaCompass.
We have 7 companies offering DL-178
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