Lidocaine Hydrochloride
- Product NDC
- 70518-2011
- 11-digit product format
- 705182011
- Labeler code
- 70518
- Product ID
- 70518-2011_dabaa612-8703-2308-e053-2a95a90aae45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207182
- Marketing category
- ANDA
- Marketing start
- 2019-04-11
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2011-0 | 70518201100 | 25 VIAL, MULTI-DOSE in 1 CARTON (70518-2011-0) > 10 mL in 1 VIAL, MULTI-DOSE (70518-2011-1) | 2019-04-11 | 0000-00-00 | No | No | Current |