Beximco Pharmaceuticals PLC
Tongi, Bangladesh · makes it
Problems found, fixed voluntarily Last FDA inspection Mar 30, 2023. 2 inspections on record.
NDC 76385-145
Flecainide Acetate 50 mg tablet
On the label: Unichem Pharmaceuticals (USA), Inc..
Where it's made
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
76385-145-0176385-145-60- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2026
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