Class II ยท Moderate risk
Docetaxel injection concentrate
Superpotent drug: over-concentrated vials of Docetaxel injection concentrate 20 mg/mL may have been distributed.
National Drug Code
Is NDC 0955-1020-01 recalled?
Docetaxel · 1 VIAL, GLASS in 1 CARTON (0955-1020-01) / 1 mL in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 0955-1020-01 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
- Docetaxel
- Strength
- DOCETAXEL 20 mg/mL
- Form
- Injection, Solution, Concentrate · Intravenous
- Labeler
- Sanofi-Aventis U.S. LLC
- Type
- Human Prescription Drug
- Product code
- 0955-1020
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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