Lidocaine Hydrochloride
- Product NDC
- 52584-066
- 11-digit product format
- 525840066
- Labeler code
- 52584
- Product ID
- 52584-066_9ab1a7d4-650c-4d25-b3af-37a90218bcbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL; INFILTRATION; PERINEURAL
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA040078
- Marketing category
- ANDA
- Marketing start
- 2010-04-01
- Marketing end
- 2021-07-01
- Substance
- LIDOCAINE HYDROCHLORIDE
- 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
- 0000-00-00
- 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 |
|---|
| 52584-066-05 | 52584006605 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-066-05) > 5 mL in 1 VIAL, SINGLE-DOSE | 2010-04-01 | 2021-07-01 | No | No | Current |