# Lidocaine Hydrochloride

NDC: 63739-997
Generic name: Lidocaine Hydrochloride
Labeler / Manufacturer: McKesson Corporation dba SKY Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20240627
Marketing ended: 20270331
FDA application: ANDA204494

## Active ingredients

- LIDOCAINE HYDROCHLORIDE: 40 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63739-997"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-997
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=903cd7bd-6c3d-4068-bb24-e91b1ca1393d