Lidocaine 51672-3020
Product NDC
51672-3020- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Ointment
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA086724
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lidocaine | 50 mg/g |
Drug Class
Amide Local Anesthetic [EPC]Antiarrhythmic [EPC]Amide Local Anesthetic [EPC]
Packaging Options(2)
1 TUBE in 1 CARTON (51672-3020-2) / 30 g in 1 TUBE
1 TUBE in 1 CARTON (51672-3020-9) / 35.44 g in 1 TUBE