Lidocaine Hydrochloride
- Product NDC
- 71872-7256
- 11-digit product format
- 718727256
- Labeler code
- 71872
- Product ID
- 71872-7256_fa3293c2-62ce-33b7-e053-6294a90a7e89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA207182
- Marketing category
- ANDA
- Marketing start
- 2017-10-30
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7256-1 | 71872725601 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7256-1) / 50 mL in 1 VIAL, MULTI-DOSE | 2021-06-30 | No | No | Historical |