# PROPAFENONE HYDROCHLORIDE

NDC: 16571-737
Generic name: PROPAFENONE HYDROCHLORIDE
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20201216

FDA application: ANDA205956

## Active ingredients

- PROPAFENONE HYDROCHLORIDE: 325 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36cf4555-6fe9-42d8-8d3b-3ca9c134a5b8