Lidocaine
- Product NDC
- 72189-493
- 11-digit product format
- 721890493
- Labeler code
- 72189
- Product ID
- 72189-493_2c4e3760-8447-4adb-e063-6394a90a5ffc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Direct_Rx
- Application
- ANDA210958
- Marketing category
- ANDA
- Marketing start
- 2023-06-22
- Substance
- LIDOCAINE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 98PI200987 | LIDOCAINE | 137-58-6 | LIDOCAINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-493-35 | 72189049335 | 35.44 g in 1 TUBE (72189-493-35) | 35.44 g | 2023-06-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lidocaine | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |