Lidocaine Hydrochloride
- Product NDC
- 55154-2373
- 11-digit product format
- 551542373
- Labeler code
- 55154
- Product ID
- 55154-2373_9a54e81c-f35d-4af2-8912-02021bf38d3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Cardinal Health
- Application
- ANDA088327
- Marketing category
- ANDA
- Marketing start
- 2010-03-30
- Marketing end
- 2019-10-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record