NDC 72789-385

Flecainide Acetate 50 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's a repackaged product: PD-Rx Pharmaceuticals, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 76385-145.

Where the pills inside were made

Beximco Pharmaceuticals PLC

Tongi, Bangladesh · makes it

Problems found, fixed voluntarily Last FDA inspection Mar 30, 2023. 2 inspections on record.

Repackaging site

• PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it

Product details

Generic drug

Flecainide: see every company that makes it

Form

tablet, oral

Strength

50 mg

Approval

ANDA ANDA210683

On the market since

Jan 11, 2024

Package NDCs

72789-385-01 72789-385-60 72789-385-93

Official label

DailyMed (National Library of Medicine), updated Feb 26, 2026

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