Inke S.A: APIs manufacturing plant.
01 1Inke S.A.
02 1MOEHS IBERICA S. L.
03 1ARAGEN LIFE SCIENCES PRIVATE LIMITED
04 1LUKASIEWICZ Research Network-INDUSTRIAL CHEMISTRY INSTITUTE
05 1Shodhana Laboratories Private Limited
01 5Carvedilol
01 2India
02 1Poland
03 2Spain
Registration Number : 218MF10100
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2019-07-26
Registration Number : 220MF10067
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2021-02-16
Registration Number : 219MF10300
Registrant's Address : 28A, IDA, Nacharam Hyderabad Telangana, India
Initial Date of Registration : 2007-09-18
Latest Date of Registration : 2007-09-18
Registration Number : 218MF10869
Registrant's Address : 8 Rydygiera Str. , 01-793 Warsaw, Poland
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2014-09-01
Registration Number : 302MF10049
Registrant's Address : 6TH FLOOR, 6B, KRISHE SAPPHIRE, SURVEY NO 88, MADHAPUR VILLAGE, SERILINGAMPALI MANDAL...
Initial Date of Registration : 2020-04-22
Latest Date of Registration : 2022-11-16
A Carvedilol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carvedilol, including repackagers and relabelers. The FDA regulates Carvedilol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carvedilol 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 Carvedilol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carvedilol supplier is an individual or a company that provides Carvedilol active pharmaceutical ingredient (API) or Carvedilol finished formulations upon request. The Carvedilol suppliers may include Carvedilol API manufacturers, exporters, distributors and traders.
click here to find a list of Carvedilol 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 Carvedilol Drug Master File in Japan (Carvedilol JDMF) empowers Carvedilol 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 Carvedilol JDMF during the approval evaluation for pharmaceutical products. At the time of Carvedilol 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 Carvedilol suppliers with JDMF on PharmaCompass.
We have 5 companies offering Carvedilol
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