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 Asclemed USA, Inc. names for other drugs.
Recalls
- Jun 8, 2026 · Class II · Asclemed USA Inc.
Lack of Assurance of Sterility
Lots: Lot #: AE3102, 121924X2, 022525X4, 033125X1, 030426X2, 033125X2, 041725X3, 061225X1, 072225X3, 080525X6, 080525X7, 080525X8, 091225X1, 100225X2, 100625X1, 122225X4, 010626X3, 041326X4, Exp 11/30/2026; AE5052, 041426X2, 041726X1, 051826X2, Exp 04/30/2028.
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
- injection, solution, infiltration
- Strength
- 10 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Feb 1, 2016
- Package NDCs
76420-715-01- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?