Lidocaine
- Product NDC
- 68788-7555
- 11-digit product format
- 687887555
- Labeler code
- 68788
- Product ID
- 68788-7555_0d920990-0c63-4d36-b095-382a475c1fa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA086724
- Marketing category
- ANDA
- Marketing start
- 1981-08-17
- 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
FDA-Initiated Inactive NDC Indexing#