NDC 71335-9753 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC71335-9753

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate ER Tablets
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211143
Marketed since
November 27, 2020
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
71335-9753-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-1)Nov 27, 2023
71335-9753-2100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-2)Jan 23, 2024
71335-9753-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-3)Aug 16, 2023
71335-9753-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-4)Apr 5, 2024
71335-9753-560 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-5)Apr 5, 2024
71335-9753-6180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-6)Apr 5, 2024
71335-9753-710 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-9753-7)Apr 5, 2024

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