# Metoprolol Tartrate

NDC: 68071-4880
Generic name: Metoprolol Tartrate
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181201

FDA application: ANDA200981

## Active ingredients

- METOPROLOL TARTRATE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4880"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4880
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87ef9aa6-2faa-0f77-e053-2a95a90a3a26