Lidocaine Hydrochloride
- Product NDC
- 70518-1894
- 11-digit product format
- 705181894
- Labeler code
- 70518
- Product ID
- 70518-1894_c4fa51c4-bf69-452e-e053-2995a90a87e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL; TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040014
- Marketing category
- ANDA
- Marketing start
- 2019-02-21
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-1894-0 | 70518189400 | 100 mL in 1 BOTTLE, PLASTIC (70518-1894-0) | 100 ml | 2019-02-21 | 0000-00-00 | No | No | Current |