NDC 72162-1856 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC72162-1856

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 (3)

Package NDCDescriptionSince
72162-1856-01000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-0)Mar 5, 2024
72162-1856-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-1)Mar 5, 2024
72162-1856-5500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-5)Mar 5, 2024

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