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
- 72611-740_ede4ae40-88e0-0536-3e01-2f2ac0b5ae3c
- Product NDC
- 72611-740
- Form
- INJECTION, SOLUTION
- Composition / generic term
- metoprolol tartrate
- Labeler
- Almaject, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200331 / 20261101
Source-listed ingredients
- METOPROLOL TARTRATE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (72611-740-10) / 5 mL in 1 VIAL, SINGLE-DOSE (72611-740-01) · 72611-740-10
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 →