Class II ยท Moderate risk
Gemcitabine Injection
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
National Drug Code
Is NDC 0143-9341-01 recalled?
Gemcitabine · 1 VIAL in 1 CARTON (0143-9341-01) / 26.3 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0143-9341-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Gemcitabine
- Strength
- GEMCITABINE HYDROCHLORIDE 38 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0143-9341
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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