Class III ยท Low risk
Ultane (sevoflurane)
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
National Drug Code
Is NDC 0074-4456-51 recalled?
Ultane · 250 mL in 1 BOTTLE, PLASTIC (0074-4456-51)
Yes — this exact package was recalled
1 FDA recall names the code 0074-4456-51 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
- Sevoflurane
- Strength
- SEVOFLURANE 250 mL/250mL
- Form
- Liquid · Respiratory (inhalation)
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0074-4456
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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