Flecainide Acetate
- Product NDC
- 60687-225
- 11-digit product format
- 606870225
- Labeler code
- 60687
- Product ID
- 60687-225_6ac218b0-2bca-242a-e053-2991aa0a0c7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flecainide Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075442
- Marketing category
- ANDA
- Marketing start
- 2016-07-18
- Marketing end
- 2019-05-31
- Substance
- FLECAINIDE ACETATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record