NDC 64980-661 – Sumatriptan

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

Human Prescription Drug

Product NDC64980-661

Product details

Brand name
Sumatriptan
Generic name
Sumatriptan
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219036
Marketed since
May 5, 2025
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 (3)

Package NDCDescriptionSince
64980-661-273 BLISTER PACK in 1 CARTON (64980-661-27) / 9 TABLET, FILM COATED in 1 BLISTER PACKMay 5, 2025
64980-661-3636 TABLET, FILM COATED in 1 BOTTLE (64980-661-36)Jul 23, 2025
64980-661-911 BLISTER PACK in 1 CARTON (64980-661-91) / 9 TABLET, FILM COATED in 1 BLISTER PACKMay 5, 2025

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