NDC 71335-2945 – Metoprolol Succinate

Metoprolol Succinate 100 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2945

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216916
Marketed since
October 2, 2023
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-2945-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-1)Oct 28, 2025
71335-2945-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-2)Oct 28, 2025
71335-2945-3120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-3)Oct 28, 2025
71335-2945-420 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-4)Oct 28, 2025
71335-2945-5100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-5)Oct 28, 2025
71335-2945-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-6)Oct 28, 2025
71335-2945-710 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-7)Oct 28, 2025

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