NDC 45963-676 – Metoprolol succinate

Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug 5 recalls

Product NDC45963-676

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204161
Marketed since
February 3, 2020
Marketing end
January 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
45963-676-11100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-11)Feb 3, 2020
45963-676-961000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-96)Feb 3, 2020

Recalls mentioning this NDC

Other Metoprolol Succinate products