# Metoprolol Succinate

NDC: 67877-593
Generic name: Metoprolol Succinate ER Tablets
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20201127

FDA application: ANDA211143

## Active ingredients

- METOPROLOL SUCCINATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-593"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-593
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58441cd3-6043-4bb8-adab-1b32a203bfb2