LT
- Product NDC
- 69420-4002
- 11-digit product format
- 694204002
- Labeler code
- 69420
- Product ID
- 69420-4002_ff00dae7-b041-4bcd-9771-df9daa3341a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine hydrochloride, triamcinolone acetonide, povidone-iodine and isopropyl alcohol
- Dosage form
- KIT
- Labeler
- SA3, LLC
- Application
- NDA014901
- Marketing category
- NDA
- Marketing start
- 2015-07-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#