Inke S.A: APIs manufacturing plant.
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01 2Inke S.A.
02 1Apitoria Pharma Private Limited
03 1Aurobindo Pharma Limited
04 1HETERO DRUGS LIMITED.
05 1Tianish Laboratories Private Limited
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01 3Eletriptan Hydrobromide
02 2Eletriptan hydrobromide
03 1Blank
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01 3India
02 2Spain
03 1U.S.A
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
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
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PharmaCompass offers a list of Eletriptan 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 Eletriptan Hydrobromide manufacturer or Eletriptan Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eletriptan Hydrobromide manufacturer or Eletriptan Hydrobromide supplier.
PharmaCompass also assists you with knowing the Eletriptan Hydrobromide API Price utilized in the formulation of products. Eletriptan Hydrobromide API Price is not always fixed or binding as the Eletriptan Hydrobromide Price is obtained through a variety of data sources. The Eletriptan Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eletriptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eletriptan, including repackagers and relabelers. The FDA regulates Eletriptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eletriptan 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eletriptan supplier is an individual or a company that provides Eletriptan active pharmaceutical ingredient (API) or Eletriptan finished formulations upon request. The Eletriptan suppliers may include Eletriptan API manufacturers, exporters, distributors and traders.
click here to find a list of Eletriptan 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 Drug Master File in Japan (Eletriptan JDMF) empowers Eletriptan 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Eletriptan 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 suppliers with JDMF on PharmaCompass.
We have 4 companies offering Eletriptan
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