Lidocaine Hydrochloride
- Product NDC
- 52584-030
- 11-digit product format
- 525840030
- Labeler code
- 52584
- Product ID
- 52584-030_c4a983d0-f641-4195-996b-5d3e5bd4f93f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- JELLY
- Route
- TOPICAL
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA086283
- Marketing category
- ANDA
- Marketing start
- 2012-06-12
- Marketing end
- 2024-02-29
- 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 |
|---|
| 52584-030-05 | 52584003005 | 1 VIAL, SINGLE-USE in 1 BAG (52584-030-05) > 5 mL in 1 VIAL, SINGLE-USE | 2012-06-12 | 0000-00-00 | No | No | Current |