IMITREX

Product NDC
0173-0449
11-digit product format
001730449
Labeler code
0173
Product ID
0173-0449_09b593bc-1a39-4a59-83da-ff02b99aabc3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sumatriptan
Dosage form
INJECTION
Route
SUBCUTANEOUS
Labeler
GlaxoSmithKline LLC
Application
NDA020080
Marketing category
NDA
Marketing start
1993-02-23
Marketing end
0000-00-00
Substance
SUMATRIPTAN SUCCINATE
Active strength
6 mg/.5mL
Pharmacologic classes
Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0173-0449-02ML - Milliliter0173-0449acdf077a-f2c9-4c25-be15-27ef68772fb512012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0173-0449-02001730449025 VIAL in 1 CARTON (0173-0449-02) > .5 mL in 1 VIAL5 vial1993-02-230000-00-00NoNoCurrent