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
55154-6886_5ee9c45a-96b4-4848-98a7-0b70bff7d730
Product NDC
55154-6886
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Metoprolol succinate
Labeler
Cardinal Health 107, LLC
Marketing category
ANDA
Marketing start / end (source format)
20120910
Source listing expiry
20261231

Source-listed ingredients

  • METOPROLOL SUCCINATE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 BLISTER PACK in 1 BAG (55154-6886-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 55154-6886-0

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 →