NDC 65862-621 – Flecainide Acetate
Flecainide Acetate 50 mg/1 · Tablet · Oral
Product NDC65862-621
Product details
- Brand name
- Flecainide Acetate
- Generic name
- Flecainide Acetate
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202821
- Marketed since
- November 3, 2017
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-621-01 | 100 TABLET in 1 BOTTLE (65862-621-01) | Nov 3, 2017 |
| 65862-621-30 | 30 TABLET in 1 BOTTLE (65862-621-30) | Nov 3, 2017 |
| 65862-621-99 | 1000 TABLET in 1 BOTTLE (65862-621-99) | Nov 3, 2017 |
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