NDC 62756-521 – sumatriptan succinate

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

Human Prescription Drug 2 recalls

Product NDC62756-521

Product details

Brand name
sumatriptan succinate
Generic name
sumatriptan succinate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078295
Marketed since
August 10, 2009
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Sumatriptan Succinate →

Package NDC codes (7)

Package NDCDescriptionSince
62756-521-013 BLISTER PACK in 1 CARTON (62756-521-01) / 9 TABLET, FILM COATED in 1 BLISTER PACKNov 1, 2020
62756-521-08100 TABLET, FILM COATED in 1 BOTTLE (62756-521-08)Aug 10, 2009
62756-521-181000 TABLET, FILM COATED in 1 BOTTLE (62756-521-18)Aug 10, 2009
62756-521-699 BLISTER PACK in 1 CARTON (62756-521-69) / 1 TABLET, FILM COATED in 1 BLISTER PACKAug 10, 2009
62756-521-8330 TABLET, FILM COATED in 1 BOTTLE (62756-521-83)Aug 10, 2009
62756-521-88100 TABLET, FILM COATED in 1 BOTTLE (62756-521-88)Aug 10, 2009
62756-521-939 BLISTER PACK in 1 CARTON (62756-521-93) / 1 TABLET, FILM COATED in 1 BLISTER PACKAug 10, 2009

Recalls mentioning this NDC

Other Sumatriptan Succinate products