NDC 53401-009 – Metoprolol succinate

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

Human Prescription Drug

Product NDC53401-009

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 · ANDA090617
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 (6)

Package NDCDescriptionSince
53401-009-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-30)May 12, 2026
53401-009-4545 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-45)May 12, 2026
53401-009-5360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-53)May 12, 2026
53401-009-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-60)May 12, 2026
53401-009-70120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-70)May 12, 2026
53401-009-80180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-009-80)May 12, 2026

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