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 Ovaprim manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ovaprim, including repackagers and relabelers. The FDA regulates Ovaprim manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ovaprim 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 Ovaprim manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ovaprim supplier is an individual or a company that provides Ovaprim active pharmaceutical ingredient (API) or Ovaprim finished formulations upon request. The Ovaprim suppliers may include Ovaprim API manufacturers, exporters, distributors and traders.
click here to find a list of Ovaprim 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 Ovaprim Drug Master File in Japan (Ovaprim JDMF) empowers Ovaprim 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 Ovaprim JDMF during the approval evaluation for pharmaceutical products. At the time of Ovaprim 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 Ovaprim suppliers with JDMF on PharmaCompass.
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