Lidocaine
- Product NDC
- 70625-400
- 11-digit product format
- 706250400
- Labeler code
- 70625
- Product ID
- 70625-400_f79c2d3a-5549-49d9-9735-0848d6146ba0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- SunGen Pharma LLC
- Application
- ANDA212486
- Marketing category
- ANDA
- Marketing start
- 2019-10-23
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record