Lidocaine Hydrochloride
- Product NDC
- 71872-7233
- 11-digit product format
- 718727233
- Labeler code
- 71872
- Product ID
- 71872-7233_fae6cc7f-7412-91e1-e053-6294a90ae3ce
- 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 |
|---|
| 71872-7233-1 | 71872723301 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7233-1) / 20 mL in 1 VIAL, MULTI-DOSE | 2020-11-17 | No | No | Historical |