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
- 71335-3167_ccca9f4b-3d0f-467a-a4a7-8505fae57d0e
- Product NDC
- 71335-3167
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metoprolol succinate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250721
- 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, EXTENDED RELEASE in 1 BOTTLE (71335-3167-1) · 71335-3167-1
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-2) · 71335-3167-2
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-3) · 71335-3167-3
- 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-4) · 71335-3167-4
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-5) · 71335-3167-5
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-6) · 71335-3167-6
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-7) · 71335-3167-7
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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