# Metoprolol Succinate

NDC: 68788-8869
Generic name: Metoprolol Succinate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250430

FDA application: ANDA216916

## Active ingredients

- METOPROLOL SUCCINATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8869"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8869
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21e18c1c-fabb-44a4-a33a-b02a47967d73