# Metoprolol Tartrate

NDC: 72611-740
Generic name: metoprolol tartrate
Labeler / Manufacturer: Almaject, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200331
Marketing ended: 20261101
FDA application: ANDA204205

## Active ingredients

- METOPROLOL TARTRATE: 1 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72611-740"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72611-740
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0370951-ab26-d4d1-b857-57518f3c4175