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
- 68382-565_2bad1abf-a566-4c58-8777-0f1a12b60690
- Product NDC
- 68382-565
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- metoprolol succinate
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180607
- 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 (68382-565-01) · 68382-565-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-565-05) · 68382-565-05
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-565-10) · 68382-565-10
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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