NDC 51672-4030 – Warfarin Sodium
Warfarin Sodium 3 mg/1 · Tablet · Oral
Product NDC51672-4030
Product details
- Brand name
- Warfarin Sodium
- Generic name
- Warfarin Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040301
- Marketed since
- July 15, 1999
- Listing expires
- December 31, 2026
- Pharmacologic class
- Vitamin K Antagonist
Active ingredients
- Warfarin Sodium 3 mg/1
Uses, dosage, side effects and warnings for Warfarin Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4030-1 | 100 TABLET in 1 BOTTLE (51672-4030-1) | Jul 15, 1999 |
| 51672-4030-3 | 1000 TABLET in 1 BOTTLE (51672-4030-3) | Jul 15, 1999 |
| 51672-4030-7 | 5000 TABLET in 1 BOTTLE (51672-4030-7) | Jul 15, 1999 |
Recalls mentioning this NDC
- D-1584-2014 Sep 24, 2014 · Class III
Failed Content Uniformity Specifications.
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