Class II ยท Moderate risk
Accucaine
Lack of Assurance of Sterility
National Drug Code
Is NDC 76420-0715-01 recalled?
Accucaine · 1 AMPULE in 1 CARTON (76420-715-01) / 5 mL in 1 AMPULE
Yes — this exact package was recalled
1 FDA recall names the code 76420-0715-01 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
- Lidocaine Hydrochloride
- Strength
- LIDOCAINE HYDROCHLORIDE 10 mg/mL
- Form
- Injection, Solution · Infiltration
- Labeler
- Asclemed USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 76420-0715
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
- 76420-0049 Estriol 3
- 76420-0634 Duloxetine 1
- 76420-0750 Dyural 40 Kit 1
- 76420-0755 Dyural 80 Kit 1
- 76420-0760 Lidolog Kit 1
Free recall alerts
Know the day your medication is recalled
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