Class II ยท Moderate risk
Zemplar (paricalcitol)
CGMP Deviations: There is potential that Abbott's third party manufacturer, Hospira, may have applied a foreign (incorrect) stopper to vials in a specific lot of Zemplar Injection.
National Drug Code
Is NDC 0074-1658-05 recalled?
Zemplar · 25 VIAL, MULTI-DOSE in 1 TRAY (0074-1658-05) / 2 mL in 1 VIAL, MULTI-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 0074-1658-05 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
- Paricalcitol
- Strength
- PARICALCITOL 5 ug/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0074-1658
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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