NDC 0173-0737 – Imitrex

Sumatriptan Succinate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0173-0737

Product details

Brand name
Imitrex
Generic name
Sumatriptan
Labeler
GlaxoSmithKline LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA020132
Marketed since
December 19, 2003
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Imitrex →

Package NDC codes (1)

Package NDCDescriptionSince
0173-0737-011 CARTON in 1 CARTON (0173-0737-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACKDec 19, 2003

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