Lidocaine Hydrochloride
- Product NDC
- 52584-713
- 11-digit product format
- 525840713
- Labeler code
- 52584
- Product ID
- 52584-713_f186defc-7833-4dbc-b8c2-aaa018e21ba6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride Anhydrous
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA080408
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- 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
- 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 |
|---|
| 52584-713-32 | 52584071332 | 1 AMPULE in 1 BAG (52584-713-32) > 2 mL in 1 AMPULE | 1 ampule | 2018-11-08 | 0000-00-00 | No | No | Current |