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
- 75907-346_9b4078bf-b309-c50b-d195-b4722dfb0945
- Product NDC
- 75907-346
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Metoprolol succinate
- Labeler
- Dr. Reddy's Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260113
- Source listing expiry
- 20271231
Source-listed ingredients
- METOPROLOL SUCCINATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-346-01) · 75907-346-01
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (75907-346-05) · 75907-346-05
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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