NDC 50090-7436 – Sumatriptan

Sumatriptan Succinate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7436

Product details

Brand name
Sumatriptan
Generic name
Sumatriptan
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078284
Marketed since
February 18, 2022
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Sumatriptan →

Package NDC codes (1)

Package NDCDescriptionSince
50090-7436-01 BLISTER PACK in 1 CARTON (50090-7436-0) / 9 TABLET, FILM COATED in 1 BLISTER PACKNov 6, 2024

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