AMERGE - 0173-0561-00 - (naratriptan hydrochloride)

Alphabetical Index


Drug Information of AMERGE

Product NDC: 0173-0561
Proprietary Name: AMERGE
Non Proprietary Name: naratriptan hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   naratriptan hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of AMERGE

Product NDC: 0173-0561
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020763
Marketing Category: NDA
Start Marketing Date: 19980226

Package Information of AMERGE

Package NDC: 0173-0561-00
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0561-00)

NDC Information of AMERGE

NDC Code 0173-0561-00
Proprietary Name AMERGE
Package Description 9 TABLET, FILM COATED in 1 BLISTER PACK (0173-0561-00)
Product NDC 0173-0561
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naratriptan hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980226
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name NARATRIPTAN HYDROCHLORIDE
Strength Number 1
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 AMERGE


General Information