NDC 0093-1721 – Warfarin Sodium
Warfarin Sodium 5 mg/1 · Tablet · Oral
Product NDC0093-1721
Product details
- Brand name
- Warfarin Sodium
- Generic name
- Warfarin Sodium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040616
- Marketed since
- April 7, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Vitamin K Antagonist
Active ingredients
- Warfarin Sodium 5 mg/1
Uses, dosage, side effects and warnings for Warfarin Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-1721-01 | 100 TABLET in 1 BOTTLE (0093-1721-01) | Apr 15, 2015 |
| 0093-1721-10 | 1000 TABLET in 1 BOTTLE (0093-1721-10) | Apr 7, 2015 |
Recalls mentioning this NDC
- D-0201-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions. - D-0200-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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