# Metoprolol Tartrate

NDC: 59651-758
Generic name: Metoprolol Tartrate
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231207

FDA application: ANDA077739

## Active ingredients

- METOPROLOL TARTRATE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-758"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-758
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac4ac150-d3e6-4bd1-8a4a-7d63fade3e49