Class II · Moderate risk
0.5% Bupivacaine HCl and Epinephrine 1:200
Lack of Assurance of Sterility; potential for vial breakage
National Drug Code
Is NDC 0409-9045-01 recalled?
Bupivacaine Hydrochloride and Epinephrine · 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-9045-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-9045-11)
Yes — this exact package was recalled
1 FDA recall names the code 0409-9045-01 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
- Bupivacaine Hydrochloride and Epinephrine
- Strength
- BUPIVACAINE HYDROCHLORIDE 5 mg/mL; EPINEPHRINE BITARTRATE 5…
- Form
- Injection, Solution · Epidural, Intracaudal, Perineural
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-9045
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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