Aurobindo Pharma Limited
Mahabubnagar, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 10, 2022. 7 inspections on record, 1 with serious problems.
NDC 57237-063
Flecainide Acetate 50 mg tablet
On the label: Rising Pharma Holdings, Inc..
Where it's made
Product details
- Generic drug
- Flecainide: see every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA202821
- On the market since
- Jul 8, 2015
- Package NDCs
57237-063-01- Official label
- DailyMed (National Library of Medicine), updated Jan 9, 2024
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