lidocaine
- Product NDC
- 70518-3972
- 11-digit product format
- 705183972
- Labeler code
- 70518
- Product ID
- 70518-3972_472b4fbc-30ee-ae27-e063-6394a90a32d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206498
- Marketing category
- ANDA
- Marketing start
- 2023-12-28
- 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 |
|---|
| 70518-3972-0 | 70518397200 | 50 g in 1 TUBE (70518-3972-0) | 50 g | 2023-12-28 | No | No | Historical |