01 1Aurobindo Pharma Limited
02 1Derivados Quimicos sau
03 1Janssen Pharmaceutica NV
04 1Janssen Pharmaceutical Sciences Unlimited Company
05 1Sri Krishna Pharmaceuticals Limited
06 1VASUDHA PHARMA CHEM LIMITED
07 1Vasudha Pharma Chem Limited
01 5Domperidone
02 1Domperidone V
03 1Japanese Pharmacopoeia domperidone
01 4India
02 1Spain
03 2U.S.A
Japanese Pharmacopoeia Domperidone
Registration Number : 226MF10135
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2014-07-02
Latest Date of Registration : 2014-07-02
Registration Number : 218MF10653
Registrant's Address : Camino Viejo de Pliego, s/n 30820 Alcantarilla Murcia Spain
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2009-04-14
Registration Number : 218MF10687
Registrant's Address : Turnhoutseweg 30 B-2340 Beerse Belgium
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 218MF10664
Registrant's Address : Little Island Industrial Estate, Little Island, Co. Cork, Ireland
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
Registration Number : 227MF10272
Registrant's Address : C-4, Industrial Area, Uppal Khalsa (V), Uppal (M), Medchal-Malkajgiri (Dist.), Hydera...
Initial Date of Registration : 2015-12-01
Latest Date of Registration : 2015-12-01
Registration Number : 304MF10034
Registrant's Address : 78/A, Bengalrao Nagar, Hyderabad-500 038, Telangana State, India.
Initial Date of Registration : 2022-02-10
Latest Date of Registration : 2022-02-10
Registration Number : 220MF10225
Registrant's Address : 78/A,Vengalrao Nagar,Hyderabad-500 038,Telangana State,INDIA
Initial Date of Registration : 2008-11-10
Latest Date of Registration : 2008-11-10
A Domperidone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Domperidone, including repackagers and relabelers. The FDA regulates Domperidone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Domperidone 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 Domperidone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Domperidone supplier is an individual or a company that provides Domperidone active pharmaceutical ingredient (API) or Domperidone finished formulations upon request. The Domperidone suppliers may include Domperidone API manufacturers, exporters, distributors and traders.
click here to find a list of Domperidone 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 Domperidone Drug Master File in Japan (Domperidone JDMF) empowers Domperidone 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 Domperidone JDMF during the approval evaluation for pharmaceutical products. At the time of Domperidone 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 Domperidone suppliers with JDMF on PharmaCompass.
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