# Metoprolol Tartrate

NDC: 0143-9660
Generic name: Metoroprolol Tartrate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20070530

FDA application: ANDA077761

## Active ingredients

- METOPROLOL TARTRATE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7ec36bb-bc6f-42de-9974-a50ac13e9410