NDC 72789-284 – Metoprolol succinate

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

Human Prescription Drug

Product NDC72789-284

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090617
Marketed since
September 10, 2012
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72789-284-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-284-30)Oct 25, 2022
72789-284-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-284-90)Jan 11, 2024

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