Lidocaine hydrochloride
- Product NDC
- 50090-7040
- 11-digit product format
- 500907040
- Labeler code
- 50090
- Product ID
- 50090-7040_f7162aa6-c335-4c18-b960-b911a2b82946
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL; TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA216780
- Marketing category
- ANDA
- Marketing start
- 2023-03-28
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V13007Z41A | LIDOCAINE HYDROCHLORIDE | 6108-05-0 | LIDOCAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7040-0 | 50090704000 | 100 mL in 1 BOTTLE (50090-7040-0) | 100 ml | 2024-01-11 | No | No | Historical |