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
- 50742-617_2613f8fb-4d2c-4e20-99b7-ccad1c745659
- Product NDC
- 50742-617
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metoprolol succinate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180206
- Source listing expiry
- 20271231
Source-listed ingredients
- METOPROLOL SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-01) · 50742-617-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-05) · 50742-617-05
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-10) · 50742-617-10
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-90) · 50742-617-90
- 32362 TABLET, EXTENDED RELEASE in 1 DRUM (50742-617-99) · 50742-617-99
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 →