AMERGE

Product NDC
0173-0561
11-digit product format
001730561
Labeler code
0173
Product ID
0173-0561_8c301e33-442e-48b9-9af9-c3afd57fa077
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
naratriptan hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
GlaxoSmithKline LLC
Application
NDA020763
Marketing category
NDA
Marketing start
1998-02-26
Marketing end
0000-00-00
Substance
NARATRIPTAN HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0173-0561-00EA - Each0173-056137a464e6-7f21-4456-851f-2f90ff12bb3512012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0173-0561-00001730561009 TABLET, FILM COATED in 1 BLISTER PACK (0173-0561-00) 1998-02-260000-00-00NoNoCurrent