NDC 63739-997
Lidocaine Hydrochloride 40 mg per 1 mL solution
On the label: McKesson Packaging Services Business Unit of McKesson Corporation.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants McKesson Packaging Services Business Unit of McKesson Corporation names for other drugs.
Recalls
- Nov 30, 2021 · Class I · Teligent Pharma, Inc.
Superpotent Drug
Lots: Lot #: 16345, Exp. Date 01/2024 - Nov 30, 2021 · Class II · Teligent Pharma, Inc.
Superpotent Drug: Minimally superpotent
Lots: Lot #: 15594, Exp Date 05/2023 - Oct 12, 2021 · Class II · Teligent Pharma, Inc.
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.
Lots: Lot #: 16306, Exp. Date 01/2024.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- solution, topical
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA204494
- On the market since
- Jun 27, 2024
- Package NDCs
63739-997-64- Official label
- DailyMed (National Library of Medicine), updated Dec 10, 2024
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