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 65862-623
Flecainide Acetate 150 mg tablet
On the label: Aurobindo Pharma Limited.
Where it's made
Product details
- Generic drug
- Flecainide: see every company that makes it
- Form
- tablet, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA202821
- On the market since
- Nov 3, 2017
- Package NDCs
65862-623-0165862-623-3065862-623-99- Official label
- DailyMed (National Library of Medicine), updated Jan 9, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?