Class II · Moderate risk
WARFARIN SODIUM Tablet
Labeling: Label Mixup; WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg) may be potentially mislabeled as SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD70636_1, EXP: 5/29/2014.
National Drug Code
Is NDC 51672-4027-01 recalled?
Warfarin Sodium · 100 TABLET in 1 BOTTLE (51672-4027-1)
Yes — this exact package was recalled
2 FDA recalls name the code 51672-4027-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Warfarin Sodium
- Strength
- WARFARIN SODIUM 1 mg/1
- Form
- Tablet · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 51672-4027
Recalls naming this package
Class II · Moderate risk
WARFARIN SODIUM Tablet
Labeling: Label Mixup; WARFARIN SODIUM, Tablet, 0.5 mg (1/2 of 1 mg) may be potentially mislabeled as SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD70636_1, EXP: 5/29/2014.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 51672-1386 Fluocinonide 3
- 51672-1351 Ciclopirox 2
- 51672-1385 Ibuprofen 2
- 51672-2130 Ibuprofen 2
- 51672-3007 Hydrocortisone and Acetic Acid 2
- 51672-4005 Carbamazepine 2
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