NDC 63629-7979 – Flecainide Acetate
Flecainide Acetate 50 mg/1 · Tablet · Oral
Product NDC63629-7979
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 50 mg/1
Uses, dosage, side effects and warnings for Flecainide Acetate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 63629-7979-1 | 30 TABLET in 1 BOTTLE (63629-7979-1) | May 9, 2019 |
| 63629-7979-2 | 60 TABLET in 1 BOTTLE (63629-7979-2) | Mar 28, 2019 |
| 63629-7979-3 | 90 TABLET in 1 BOTTLE (63629-7979-3) | Jan 7, 2021 |
| 63629-7979-4 | 10 TABLET in 1 BOTTLE (63629-7979-4) | Apr 3, 2024 |
| 63629-7979-5 | 180 TABLET in 1 BOTTLE (63629-7979-5) | Sep 28, 2022 |
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