Class III ยท Low risk
Lidolog Kit
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
National Drug Code
Is NDC 76420-0760-01 recalled?
Lidolog Kit · 1 KIT in 1 CARTON (76420-760-01) * 25 VIAL in 1 CARTON (70121-1049-5) / 1 mL in 1 VIAL * .9 mL in 1 PACKET (67777-419-02) * 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-164-02) / 2 mL in 1 VIAL, SIN
Yes — this exact package was recalled
1 FDA recall names the code 76420-0760-01 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, kenalog, povidone iodine
- Form
- Kit · Epidural, Infiltration, Intra-Articular, Intramuscular, Topical
- Labeler
- Asclemed USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 76420-0760
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
- 76420-0715 Accucaine 1
- 76420-0750 Dyural 40 Kit 1
- 76420-0755 Dyural 80 Kit 1
Free recall alerts
Know the day your medication is recalled
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