NDC 72603-144 – Metoprolol succinate

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

Human Prescription Drug

Product NDC72603-144

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Northstar Rx LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078889
Marketed since
April 10, 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 (3)

Package NDCDescriptionSince
72603-144-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-01)Apr 10, 2023
72603-144-02500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-02)Apr 10, 2023
72603-144-031000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-03)Sep 12, 2023

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