NDC 68788-8619 – Sumatriptan

Sumatriptan Succinate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-8619

Product details

Brand name
Sumatriptan
Generic name
Sumatriptan
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078284
Marketed since
March 29, 2024
Listing expires
December 31, 2027
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
68788-8619-91 BLISTER PACK in 1 CARTON (68788-8619-9) / 9 TABLET, FILM COATED in 1 BLISTER PACKMar 29, 2024

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