Home > National Drug Code (NDC) > Sumatriptan

Sumatriptan - 63304-098-13 - (Sumatriptan)

Alphabetical Index


Drug Information of Sumatriptan

Product NDC: 63304-098
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: 63304-098
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076554
Marketing Category: ANDA
Start Marketing Date: 20090813

Package Information of Sumatriptan

Package NDC: 63304-098-13
Package Description: 120 TABLET in 1 BOTTLE (63304-098-13)

NDC Information of Sumatriptan

NDC Code 63304-098-13
Proprietary Name Sumatriptan
Package Description 120 TABLET in 1 BOTTLE (63304-098-13)
Product NDC 63304-098
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 Ranbaxy Pharmaceuticals Inc.
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


General Information