# Metoprolol Tartrate

NDC: 68645-191
Generic name: Metoprolol Tartrate
Labeler / Manufacturer: Legacy Pharmaceutical Packaging, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070911
Marketing ended: 20270731
FDA application: ANDA077739

## Active ingredients

- METOPROLOL TARTRATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68645-191"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68645-191
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20cc66c0-a00b-4643-9819-6e0daed51e5f