Class III · Low risk
Enoxaparin Sodium
Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL
National Drug Code
Is NDC 0955-1012-10 recalled?
Enoxaparin sodium · 10 CELLO PACK in 1 CARTON (0955-1012-10) / 1 SYRINGE in 1 CELLO PACK (0955-1012-01) / .8 mL in 1 SYRINGE
Yes — this exact package was recalled
1 FDA recall names the code 0955-1012-10 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
- enoxaparin sodium
- Strength
- ENOXAPARIN SODIUM 120 mg/.8mL
- Form
- Injection · Subcutaneous
- Labeler
- Sanofi-Aventis U.S. LLC
- Type
- Human Prescription Drug
- Product code
- 0955-1012
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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