# Lidocaine Hydrochloride

NDC: 51672-1411
Generic name: Lidocaine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20231208

FDA application: ANDA218182

## Active ingredients

- LIDOCAINE HYDROCHLORIDE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1411"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1411
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=845b96c1-36a3-431f-8316-112ae881d934
