Lidocaine Hydrochloride
- Product NDC
- 55154-6969
- 11-digit product format
- 551546969
- Labeler code
- 55154
- Product ID
- 55154-6969_4fda95bc-84c7-4dea-9178-a0852507eda7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INFILTRATION; PERINEURAL
- Labeler
- Cardinal Health
- Application
- ANDA088327
- Marketing category
- ANDA
- Marketing start
- 2010-03-30
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record