Hexicinide
- Product NDC
- 59088-748
- 11-digit product format
- 590880748
- Labeler code
- 59088
- Product ID
- 59088-748_a1002b13-4fb9-1b20-e053-2995a90a6cad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hexicinide
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- ANDA090256
- Marketing category
- ANDA
- Marketing start
- 2014-01-14
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record