Class II ยท Moderate risk
Sterile Diluent
CGMP Deviations
National Drug Code
Is NDC 0002-0800-01 recalled?
diluent · 1 VIAL in 1 CARTON (0002-0800-01) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0002-0800-01 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
- diluent
- Strength
- WATER 1 mL/mL
- Form
- Injection, Solution
- Labeler
- Eli Lilly and Company
- Type
- Drug for Further Processing
- Product code
- 0002-0800
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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