# metoprolol succinate

NDC: 68382-567
Generic name: metoprolol succinate
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180607

FDA application: ANDA203894

## 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:"68382-567"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-567
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd77ec6e-c58c-440b-81d6-8a462b2fdc9c