# METOPROLOL TARTRATE

NDC: 69367-355
Generic name: metoprolol tartrate
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231218
Marketing ended: 20260731
FDA application: ANDA074453

## Active ingredients

- METOPROLOL TARTRATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-355"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-355
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d352c34-47f8-4662-9ac5-d5a32bd1660f