# Metoprolol Tartrate

NDC: 43063-821
Generic name: Metoprolol Tartrate
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070911
Marketing ended: 20270831
FDA application: ANDA077739

## Active ingredients

- METOPROLOL TARTRATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-821"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-821
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19678edf-934a-45f3-b5da-94d10e9b3248