Lidocaine Hydrochloride
- Product NDC
- 68788-9799
- 11-digit product format
- 687889799
- Labeler code
- 68788
- Product ID
- 68788-9799_59a374f1-0ad6-4707-b140-adb20f6550d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL; TOPICAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040014
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- 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
- 2023-12-31
- 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 |
|---|
| 68788-9799-1 | 68788979901 | 100 mL in 1 BOTTLE, PLASTIC (68788-9799-1) | 100 ml | 2012-04-30 | 0000-00-00 | No | No | Current |