# Flecainide Acetate

NDC: 62135-660
Generic name: Flecainide Acetate
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090709

FDA application: ANDA079164

## Active ingredients

- FLECAINIDE ACETATE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a604aee4-30d5-4007-9882-98137d0d867f