Lidocaine Hydrochloride
- Product NDC
- 71872-7301
- 11-digit product format
- 718727301
- Labeler code
- 71872
- Product ID
- 71872-7301_fa19aa30-e94d-6f5d-e053-6294a90aaff0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA083158
- Marketing category
- ANDA
- Marketing start
- 2005-12-01
- 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 |
|---|
| 71872-7301-1 | 71872730101 | 1 CARTON in 1 BAG (71872-7301-1) / 1 SYRINGE in 1 CARTON / 5 mL in 1 SYRINGE | 1 carton | 2023-02-14 | No | No | Historical |