United States · FDA National Drug Code directory

Metoprolol succinate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
53401-014_56444582-2b3c-afdd-e063-6394a90a5e64
Product NDC
53401-014
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Metoprolol succinate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20260113
Source listing expiry
20271231

Source-listed ingredients

  • METOPROLOL SUCCINATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-30) · 53401-014-30
  • 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-45) · 53401-014-45
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-53) · 53401-014-53
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-60) · 53401-014-60
  • 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53401-014-80) · 53401-014-80

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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