# Metoprolol Succinate

NDC: 51655-203
Generic name: Metoprolol succinate
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200901

FDA application: ANDA204106

## Active ingredients

- METOPROLOL SUCCINATE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-203"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-203
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c213c327-68b7-da5b-e053-2a95a90a4028