United States · FDA National Drug Code directory
Metoprolol Tartrate
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
- 82804-978_de781298-37cb-4c03-8431-b6d86ffbde0d
- Product NDC
- 82804-978
- Form
- TABLET
- Composition / generic term
- Metoprolol Tartrate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231102
- Source listing expiry
- 20261231
Source-listed ingredients
- METOPROLOL TARTRATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (82804-978-00) · 82804-978-00
- 1000 TABLET in 1 BOTTLE (82804-978-11) · 82804-978-11
- 30 TABLET in 1 BOTTLE (82804-978-30) · 82804-978-30
- 500 TABLET in 1 BOTTLE (82804-978-55) · 82804-978-55
- 60 TABLET in 1 BOTTLE (82804-978-60) · 82804-978-60
- 90 TABLET in 1 BOTTLE (82804-978-90) · 82804-978-90
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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