LIDOCAINE HYDROCHLORIDE
- Product NDC
- 51662-1551
- 11-digit product format
- 516621551
- Labeler code
- 51662
- Product ID
- 51662-1551_10356612-76d5-72cf-e063-6394a90a1ecb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- JELLY
- Route
- TOPICAL
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA086283
- Marketing category
- ANDA
- Marketing start
- 2021-06-14
- 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 |
|---|
| 51662-1551-3 | 51662155103 | 25 POUCH in 1 CASE (51662-1551-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1551-2) / 20 mL in 1 VIAL, SINGLE-USE | 25 pouch | 2021-06-14 | No | No | Historical |