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
- 71335-3134_2eb3bca1-30be-4a8f-88b2-123033473f90
- Product NDC
- 71335-3134
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Metoprolol succinate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120910
- Source listing expiry
- 20271231
Source-listed ingredients
- METOPROLOL SUCCINATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-1) · 71335-3134-1
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3134-2) · 71335-3134-2
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 →