Lidocaine Hydrochloride
- Product NDC
- 70518-2649
- 11-digit product format
- 705182649
- Labeler code
- 70518
- Product ID
- 70518-2649_dc7701b5-0c47-b4df-e053-2a95a90a0f1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA088329
- Marketing category
- ANDA
- Marketing start
- 2020-03-25
- 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 |
|---|
| 70518-2649-0 | 70518264900 | 25 VIAL, SINGLE-DOSE in 1 TRAY (70518-2649-0) > 30 mL in 1 VIAL, SINGLE-DOSE (70518-2649-1) | 2020-03-25 | 0000-00-00 | No | No | Current |