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
- 45963-676_a7e9a234-a8a6-4afe-ba8e-d569772bc39a
- Product NDC
- 45963-676
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- metoprolol succinate
- Labeler
- Actavis Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200203 / 20270131
Source-listed ingredients
- METOPROLOL SUCCINATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-11) · 45963-676-11
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-96) · 45963-676-96
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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