# Mirabegron

NDC: 69238-2861
Generic name: Mirabegron
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260419

FDA application: ANDA218543

## Active ingredients

- MIRABEGRON: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69238-2861"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-2861
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e597023d-6dcc-4d9e-8ce0-2d28a5d862f3