Inke S.A: APIs manufacturing plant.
01 2Inke S.A.
02 1Apitoria Pharma Private Limited
03 1Aurobindo Pharma Limited
04 1HETERO DRUGS LIMITED.
05 1Tianish Laboratories Private Limited
01 3Eletriptan Hydrobromide
02 2Eletriptan hydrobromide
03 1Blank
01 3India
02 2Spain
03 1U.S.A
Inke S.A: APIs manufacturing plant.
Registration Number : 304MF10075
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2022-05-18
Latest Date of Registration : 2022-05-18
Inke S.A: APIs manufacturing plant.
Registration Number : 229MF10147
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2017-07-31
Latest Date of Registration : 2017-07-31
Registration Number : 229MF10175
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Telangana, India
Initial Date of Registration : 2017-09-04
Latest Date of Registration : 2017-09-04
Eletriptan hydrobromide "Apitoria"
Registration Number : 306MF10085
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 : 306MF10042
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2024-03-13
Latest Date of Registration : 2024-03-13
Registration Number : 229MF10075
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2017-04-07
Latest Date of Registration : 2017-04-07
A Eletriptan Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eletriptan Hydrobromide, including repackagers and relabelers. The FDA regulates Eletriptan Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eletriptan Hydrobromide 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 Eletriptan Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eletriptan Hydrobromide supplier is an individual or a company that provides Eletriptan Hydrobromide active pharmaceutical ingredient (API) or Eletriptan Hydrobromide finished formulations upon request. The Eletriptan Hydrobromide suppliers may include Eletriptan Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Eletriptan Hydrobromide 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 Eletriptan Hydrobromide Drug Master File in Japan (Eletriptan Hydrobromide JDMF) empowers Eletriptan Hydrobromide 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 Eletriptan Hydrobromide JDMF during the approval evaluation for pharmaceutical products. At the time of Eletriptan Hydrobromide 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 Eletriptan Hydrobromide suppliers with JDMF on PharmaCompass.
We have 4 companies offering Eletriptan Hydrobromide
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