NDC 71335-2995 – Flecainide Acetate
Flecainide Acetate 50 mg/1 · Tablet · Oral
Product NDC71335-2995
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 50 mg/1
Uses, dosage, side effects and warnings for Flecainide Acetate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2995-1 | 30 TABLET in 1 BOTTLE (71335-2995-1) | Feb 4, 2026 |
| 71335-2995-2 | 60 TABLET in 1 BOTTLE (71335-2995-2) | Feb 4, 2026 |
| 71335-2995-3 | 90 TABLET in 1 BOTTLE (71335-2995-3) | Feb 4, 2026 |
| 71335-2995-4 | 10 TABLET in 1 BOTTLE (71335-2995-4) | Feb 4, 2026 |
| 71335-2995-5 | 180 TABLET in 1 BOTTLE (71335-2995-5) | Feb 4, 2026 |
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