NDC 71351-027
Lidocaine Hydrochloride 20 mg per 1 mL solution
On the label: Brookfield Pharmaceuticals, LLC..
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 Brookfield Pharmaceuticals, LLC. names for other drugs.
Recalls
- Apr 2, 2026 · Class II · Huons Co., Ltd.
Lack of Assurance of Sterility
Lots: All lots within expiry - Apr 2, 2026 · Class II · Huons Co., Ltd.
Lack of Assurance of Sterility
Lots: All lots within expiry
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, intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA212821
- On the market since
- Nov 27, 2025
- Package NDCs
71351-027-2071351-027-25- Official label
- DailyMed (National Library of Medicine), updated Nov 27, 2025
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