NDC 71335-2592 – Metoprolol Succinate

Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2592

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 (6)

Package NDCDescriptionSince
71335-2592-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-1)Jun 4, 2025
71335-2592-230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-2)Jun 4, 2025
71335-2592-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-3)Jun 4, 2025
71335-2592-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-4)Jun 4, 2025
71335-2592-560 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-5)Jun 4, 2025
71335-2592-610 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2592-6)Jun 4, 2025

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