# Flecainide Acetate

NDC: 0054-0010
Generic name: flecainide acetate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20030114

FDA application: ANDA076278

## Active ingredients

- FLECAINIDE ACETATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f6b78d4-8ac8-464b-bb78-ee70cbc97898