Lidocaine
- Product NDC
- 70518-2147
- 11-digit product format
- 705182147
- Labeler code
- 70518
- Product ID
- 70518-2147_e38d4ae6-1947-8b14-e053-2995a90a3d7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207810
- Marketing category
- ANDA
- Marketing start
- 2019-06-14
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2147-0 | 70518214700 | 1 TUBE in 1 CARTON (70518-2147-0) > 50 g in 1 TUBE | 1 tube | 2019-06-14 | 0000-00-00 | No | No | Current |