# Propafenone Hydrochloride

NDC: 0832-0740
Generic name: Propafenone Hydrochloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200625
Marketing ended: 20261130
FDA application: ANDA212744

## Active ingredients

- PROPAFENONE HYDROCHLORIDE: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-0740"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-0740
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8aa6f58a-2980-4caa-9c54-d55d69d5d132