NDC 71335-2523 – Flecainide Acetate
Flecainide Acetate 150 mg/1 · Tablet · Oral
Product NDC71335-2523
Product details
- Brand name
- Flecainide Acetate
- Generic name
- Flecainide acetate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA215599
- Marketed since
- September 15, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Flecainide Acetate 150 mg/1
Uses, dosage, side effects and warnings for Flecainide Acetate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2523-1 | 30 TABLET in 1 BOTTLE (71335-2523-1) | Nov 25, 2024 |
| 71335-2523-2 | 90 TABLET in 1 BOTTLE (71335-2523-2) | Nov 25, 2024 |
| 71335-2523-3 | 60 TABLET in 1 BOTTLE (71335-2523-3) | Nov 25, 2024 |
| 71335-2523-4 | 180 TABLET in 1 BOTTLE (71335-2523-4) | Nov 25, 2024 |
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