NDC 71335-2172 – Flecainide Acetate
Flecainide Acetate 150 mg/1 · Tablet · Oral
Product NDC71335-2172
Product details
- Brand name
- Flecainide Acetate
- Generic name
- Flecainide Acetate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202821
- Marketed since
- July 8, 2015
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 71335-2172-1 | 30 TABLET in 1 BOTTLE (71335-2172-1) | Oct 3, 2022 |
| 71335-2172-2 | 90 TABLET in 1 BOTTLE (71335-2172-2) | Oct 3, 2022 |
| 71335-2172-3 | 60 TABLET in 1 BOTTLE (71335-2172-3) | Oct 3, 2022 |
| 71335-2172-4 | 180 TABLET in 1 BOTTLE (71335-2172-4) | Oct 3, 2022 |
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