Lidocaine Hydrochloride
- Product NDC
- 52584-323
- 11-digit product format
- 525840323
- Labeler code
- 52584
- Product ID
- 52584-323_de9e9e16-432b-41b0-82c2-e8b2af82651f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA040302
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- Marketing end
- 2023-06-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-323-05 | 52584032305 | 1 CARTON in 1 BAG (52584-323-05) > 1 SYRINGE in 1 CARTON > 5 mL in 1 SYRINGE | 1 carton | 2010-09-01 | 0000-00-00 | No | No | Current |