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