Lidocaine hydrochloride
- Product NDC
- 17856-8138
- 11-digit product format
- 178568138
- Labeler code
- 17856
- Product ID
- 17856-8138_401eca82-6f41-2006-e063-6394a90a6421
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL; TOPICAL
- Labeler
- Atlantic Biologicals Corp.
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lidocaine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1010739 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-8138-1 | Lidocaine hydrochloride | 15 mL in 1 CUP, UNIT-DOSE | SOLUTION | 15 | | 1 |
| 17856-8138-1 | Lidocaine hydrochloride | 50 in 1 CASE | SOLUTION | 50 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 17856-8138-1 | 17856813801 | 50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1) / 15 mL in 1 CUP, UNIT-DOSE | 2025-10-01 | No | No | Historical |