Panretin
- Product NDC
- 62856-601
- 11-digit product format
- 628560601
- Labeler code
- 62856
- Product ID
- 62856-601_a08edeb2-af0b-4ee6-928c-a7a21ad03725
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alitretinoin
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Eisai Inc.
- Application
- NDA020886
- Marketing category
- NDA
- Marketing start
- 2009-02-03
- Marketing end
- 2021-10-31
- Substance
- ALITRETINOIN
- Active strength
- 60 mg/60g
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62856-601-22 | 62856060122 | 60 g in 1 TUBE (62856-601-22) | 60 g | 2009-02-03 | 2021-10-31 | No | No | Current |