NDC 0054-0010

Flecainide Acetate 50 mg tablet

On the label: Hikma Pharmaceuticals USA Inc..

Where it's made

West-Ward Columbus Inc.

Columbus, OH, United States · makes it

No problems found Last FDA inspection Apr 30, 2026. 27 inspections on record.

Product details

Generic drug
Flecainide: see every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA076278
On the market since
Jan 14, 2003
Package NDCs
0054-0010-20 0054-0010-21 0054-0010-25
Official label
DailyMed (National Library of Medicine), updated Dec 4, 2024

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