IMITREX - 0173-0736-01 - (sumatriptan succinate)

Alphabetical Index


Drug Information of IMITREX

Product NDC: 0173-0736
Proprietary Name: IMITREX
Non Proprietary Name: sumatriptan succinate
Active Ingredient(s): 50    mg/1 & nbsp;   sumatriptan succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of IMITREX

Product NDC: 0173-0736
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020132
Marketing Category: NDA
Start Marketing Date: 20031217

Package Information of IMITREX

Package NDC: 0173-0736-01
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0736-01)

NDC Information of IMITREX

NDC Code 0173-0736-01
Proprietary Name IMITREX
Package Description 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0736-01)
Product NDC 0173-0736
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20031217
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
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 IMITREX


General Information