01 1Gedeon Richter Plc.
02 2HETERO DRUGS LIMITED.
03 2LUPIN LIMITED.
04 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
01 1LISINOPRIL DIHYDRATE
02 1Lisinopril
03 2Lisinopril Hydrate
04 1Lisinopril SN
05 1Lisinopril hydrate
01 1China
02 1Hungary
03 4India
Registration Number : 219MF10198
Registrant's Address : Budapest, Gyomroi ut 19-21, Hungary, H-1103
Initial Date of Registration : 2007-06-08
Latest Date of Registration : 2007-06-08
Registration Number : 222MF10145
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2010-04-22
Latest Date of Registration : 2010-04-22
Registration Number : 218MF10592
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Andhra...
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
Registration Number : 218MF10860
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2008-07-10
Registration Number : 301MF10069
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2019-09-20
Latest Date of Registration : 2019-09-20
Registration Number : 219MF10148
Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2019-05-21
A Lisinopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lisinopril, including repackagers and relabelers. The FDA regulates Lisinopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lisinopril 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 Lisinopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lisinopril supplier is an individual or a company that provides Lisinopril active pharmaceutical ingredient (API) or Lisinopril finished formulations upon request. The Lisinopril suppliers may include Lisinopril API manufacturers, exporters, distributors and traders.
click here to find a list of Lisinopril 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 Lisinopril Drug Master File in Japan (Lisinopril JDMF) empowers Lisinopril 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 Lisinopril JDMF during the approval evaluation for pharmaceutical products. At the time of Lisinopril 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 Lisinopril suppliers with JDMF on PharmaCompass.
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