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Sumatriptan - 50436-4623-1 - (Sumatriptan)

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Drug Information of Sumatriptan

Product NDC: 50436-4623
Proprietary Name: Sumatriptan
Non Proprietary Name: Sumatriptan
Active Ingredient(s): 50    mg/1 & nbsp;   Sumatriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan

Product NDC: 50436-4623
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076554
Marketing Category: ANDA
Start Marketing Date: 20090813

Package Information of Sumatriptan

Package NDC: 50436-4623-1
Package Description: 9 TABLET in 1 BOTTLE (50436-4623-1)

NDC Information of Sumatriptan

NDC Code 50436-4623-1
Proprietary Name Sumatriptan
Package Description 9 TABLET in 1 BOTTLE (50436-4623-1)
Product NDC 50436-4623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090813
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of Sumatriptan


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