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
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PharmaCompass offers a list of Galantamine Hydrobromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Galantamine Hydrobromide API Price utilized in the formulation of products. Galantamine Hydrobromide API Price is not always fixed or binding as the Galantamine Hydrobromide Price is obtained through a variety of data sources. The Galantamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A G1660_SIGMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of G1660_SIGMA, including repackagers and relabelers. The FDA regulates G1660_SIGMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. G1660_SIGMA API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A G1660_SIGMA supplier is an individual or a company that provides G1660_SIGMA active pharmaceutical ingredient (API) or G1660_SIGMA finished formulations upon request. The G1660_SIGMA suppliers may include G1660_SIGMA API manufacturers, exporters, distributors and traders.
click here to find a list of G1660_SIGMA 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 G1660_SIGMA Drug Master File in Japan (G1660_SIGMA JDMF) empowers G1660_SIGMA 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 G1660_SIGMA JDMF during the approval evaluation for pharmaceutical products. At the time of G1660_SIGMA JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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