Class II · Moderate risk
Fosphenytoin Sodium Injection
Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.
National Drug Code
Is NDC 0143-9782-10 recalled?
Fosphenytoin Sodium · 10 VIAL in 1 PACKAGE (0143-9782-10) / 10 mL in 1 VIAL (0143-9782-01)
Yes — this exact package was recalled
1 FDA recall names the code 0143-9782-10 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
- Fosphenytoin Sodium
- Strength
- FOSPHENYTOIN SODIUM 50 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- West-Ward Pharmaceuticals Corp
- Type
- Human Prescription Drug
- Product code
- 0143-9782
Recalls naming this package
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
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