NDC 53401-014 – Metoprolol succinate

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

Human Prescription Drug

Product NDC53401-014

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078889
Marketed since
January 13, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
53401-014-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-30)May 26, 2026
53401-014-4545 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-45)Jul 9, 2026
53401-014-5360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-53)May 26, 2026
53401-014-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-60)May 26, 2026
53401-014-80180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-80)May 26, 2026

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