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
67296-2325_5a65a65c-974b-5756-e063-6294a90a7861
Product NDC
67296-2325
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Metoprolol succinate
Labeler
Redpharm Drug
Marketing category
ANDA
Marketing start / end (source format)
20230410
Source listing expiry
20271231

Source-listed ingredients

  • METOPROLOL SUCCINATE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2325-6) · 67296-2325-6

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →