Class II · Moderate risk
Lidocaine Hydrochloride
Superpotent Drug: Minimally superpotent
National Drug Code
Is NDC 63739-0997-64 recalled?
Lidocaine Hydrochloride · 1 BOTTLE in 1 CARTON (63739-997-64) / 50 mL in 1 BOTTLE
Yes — this exact package was recalled
3 FDA recalls name the code 63739-0997-64 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.
2 of these recalls are still ongoing.
- Active ingredient
- Lidocaine Hydrochloride
- Strength
- LIDOCAINE HYDROCHLORIDE 40 mg/mL
- Form
- Solution · Topical
- Labeler
- McKesson Corporation dba SKY Packaging
- Type
- Human Prescription Drug
- Product code
- 63739-0997
Recalls naming this package
Class I · High risk
Lidocaine Hydrochloride
Superpotent Drug
Class II · Moderate risk
Lidocaine Hydrochloride Topical Solution USP 4%
CGMP Deviations: Lots recalled because they were manufactured at the same facility using the same components as the products that had cracked seals in caps that were found to be superpotent.
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
- 63739-0053 See recall 2
- 63739-0434 See recall 2
- 63739-0549 See recall 2
- 63739-0996 See recall 2
- 63739-0998 See recall 2
- 63739-0014 See recall 1
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