Lidocaine Hydrochloride 51672-1411
Product NDC
51672-1411- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Solution
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- December 8, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA218182
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lidocaine Hydrochloride | 40 mg/mL |
Drug Class
Amide Local Anesthetic [EPC]Amides [CS]Antiarrhythmic [EPC]
Packaging Options(1)
1 BOTTLE in 1 CARTON (51672-1411-3) / 50 mL in 1 BOTTLE