# Lidocaine

NDC: 51672-3008
Generic name: Lidocaine
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 19810817

FDA application: ANDA086724

## Active ingredients

- LIDOCAINE: 50 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-3008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-3008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5eb2c62f-5352-41d7-bd66-c65b1988a9ab