# Metoprolol Succinate

NDC: 72789-497
Generic name: Metoprolol Succinate
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220427

FDA application: ANDA207206

## Active ingredients

- METOPROLOL TARTRATE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-497"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-497
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d8cdd8b-3896-4cd0-9570-a6f4e1d340d7