Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 66467-9730-05 recalled?

Lidocaine · 50 CARTRIDGE in 1 CARTON (66467-9730-5) / 1.7 mL in 1 CARTRIDGE

Yes — this exact package was recalled

1 FDA recall names the code 66467-9730-05 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
Lidocaine Hydrochloride and Epinephrine Bitartrate
Strength
LIDOCAINE HYDROCHLORIDE 20 mg/mL; EPINEPHRINE BITARTRATE…
Form
Injection, Solution · Submucosal
Labeler
Darby Dental Supply, LLC
Type
Human Prescription Drug
Product code
66467-9730

Recalls naming this package

Class II · Moderate risk

Lidocaine Hydrochloride 2% and Epinephrine 1:100

Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000 Injectable, distributed under the names: Octocaine 100, and 2% Xylocaine Dental, may be subpotent for the epinephrine component.

Terminated Wrong potency / content Novocol Pharmaceutical of Canada D-923-2013

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