IMITREX - 0173-0524-00 - (sumatriptan)

Alphabetical Index


Drug Information of IMITREX

Product NDC: 0173-0524
Proprietary Name: IMITREX
Non Proprietary Name: sumatriptan
Active Ingredient(s): 5    mg/1 & nbsp;   sumatriptan
Administration Route(s): NASAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of IMITREX

Product NDC: 0173-0524
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020626
Marketing Category: NDA
Start Marketing Date: 19971010

Package Information of IMITREX

Package NDC: 0173-0524-00
Package Description: 6 CONTAINER in 1 BOX (0173-0524-00) > 1 SPRAY in 1 CONTAINER

NDC Information of IMITREX

NDC Code 0173-0524-00
Proprietary Name IMITREX
Package Description 6 CONTAINER in 1 BOX (0173-0524-00) > 1 SPRAY in 1 CONTAINER
Product NDC 0173-0524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan
Dosage Form Name SPRAY
Route Name NASAL
Start Marketing Date 19971010
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name SUMATRIPTAN
Strength Number 5
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