01 1Apitoria Pharma Private Limited
02 1JUBILANT PHARMOVA LIMITED
03 1ScinoPharm Taiwan, Ltd.
04 1TAPI Czech Industries s. r. o.
01 1Galantamine Hydrobromide
02 1Galantamine hydrobromide
03 1Galantamine hydrobromide
04 1Blank
01 2India
02 1Israel
03 1Taiwan
Galantamine hydrobromide "Apitoria"
Registration Number : 306MF10088
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad, Telangana, INDIA.
Initial Date of Registration : 2024-07-03
Latest Date of Registration : 2024-07-03
Registration Number : 231MF10054
Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2019-02-21
Latest Date of Registration : 2019-02-21
Registration Number : 230MF10065
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
Initial Date of Registration : 2018-05-15
Latest Date of Registration : 2022-01-26
Galantamine hydrobromide (Teva)
Registration Number : 231MF10027
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2019-02-05
Latest Date of Registration : 2019-02-05
A Galantamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Galantamine, including repackagers and relabelers. The FDA regulates Galantamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Galantamine 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 Galantamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Galantamine supplier is an individual or a company that provides Galantamine active pharmaceutical ingredient (API) or Galantamine finished formulations upon request. The Galantamine suppliers may include Galantamine API manufacturers, exporters, distributors and traders.
click here to find a list of Galantamine 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 Galantamine Drug Master File in Japan (Galantamine JDMF) empowers Galantamine 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 Galantamine JDMF during the approval evaluation for pharmaceutical products. At the time of Galantamine 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 Galantamine suppliers with JDMF on PharmaCompass.
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