lidocaine hydrochloride
- Product NDC
- 71872-7362
- 11-digit product format
- 718727362
- Labeler code
- 71872
- Product ID
- 71872-7362_4643070f-6826-c636-e063-6394a90a4d46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA219535
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 10 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 | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1010033 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7362-1 | lidocaine hydrochloride | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 1 |
| 71872-7362-1 | lidocaine hydrochloride | 50 mL in 1 VIAL, MULTI-DOSE | INJECTION, 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 |
|---|
| 71872-7362-1 | 71872736201 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7362-1) / 50 mL in 1 VIAL, MULTI-DOSE | 2025-11-05 | No | No | Historical |