Lidocaine
- Product NDC
- 0143-9172
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA080407
- Marketing category
- ANDA
- Substance
- LIDOCAINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 0143-9172-10 | 10 VIAL, MULTI-DOSE in 1 CARTON (0143-9172-10) / 20 mL in 1 VIAL, MULTI-DOSE (0143-9172-01) | 2025-05-20 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| These highlights do not include all the information needed to use [Product Name] safely and effectively. See full prescribing information for [Product Name]. [Product Name] ([Established Name]) [Dosage Form] for [Route of Administration] use Initial U.S. Approval: [Year] | Hikma Pharmaceuticals USA Inc. | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 6 |