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
- 68788-8312_cbe0e043-d578-4a7f-9b88-68569f300b1d
- Product NDC
- 68788-8312
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- metoprolol succinate
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221220
- Source listing expiry
- 20271231
Source-listed ingredients
- METOPROLOL SUCCINATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8312-1) · 68788-8312-1
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8312-3) · 68788-8312-3
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8312-6) · 68788-8312-6
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8312-9) · 68788-8312-9
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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