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
82804-165_3c43fe89-2283-482e-9d97-648d3ed183f8
Product NDC
82804-165
Form
TABLET, FILM COATED
Composition / generic term
Metoprolol Tartrate
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20181201
Source listing expiry
20261231

Source-listed ingredients

  • METOPROLOL TARTRATE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90) · 82804-165-90

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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