Lidocaine Hydrochloride
- Product NDC
- 50090-5667
- 11-digit product format
- 500905667
- Labeler code
- 50090
- Product ID
- 50090-5667_0ebb364e-458b-42b6-afe7-692669e4d20f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- SOLUTION
- Route
- OROPHARYNGEAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040708
- Marketing category
- ANDA
- Marketing start
- 2007-02-27
- 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 |
|---|
| 50090-5667-0 | 50090566700 | 100 mL in 1 BOTTLE (50090-5667-0) | 100 ml | 2021-09-15 | 0000-00-00 | No | No | Current |