Lidocaine
- Product NDC
- 68788-6335
- 11-digit product format
- 687886335
- Labeler code
- 68788
- Product ID
- 68788-6335_8d90096d-8b33-4cca-a150-b12c646ec8b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA086724
- Marketing category
- ANDA
- Marketing start
- 2019-03-06
- 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