NDC 71335-3134 – Metoprolol succinate

Metoprolol Succinate 200 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-3134

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 · ANDA078889
Marketed since
September 10, 2012
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71335-3134-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-1)May 21, 2026
71335-3134-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-2)May 21, 2026

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