Lidocaine
- Product NDC
- 71335-2856
- 11-digit product format
- 713352856
- Labeler code
- 71335
- Product ID
- 71335-2856_226083f0-f913-4b90-9035-84945d51ee4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212695
- Marketing category
- ANDA
- Marketing start
- 2021-04-20
- 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 |
|---|
| 71335-2856-1 | 71335285601 | 1 TUBE in 1 CARTON (71335-2856-1) / 35.44 g in 1 TUBE | 1 tube | 2025-11-11 | No | No | Historical |