Verdeso
- Product NDC
- 16110-111
- 11-digit product format
- 161100111
- Labeler code
- 16110
- Product ID
- 16110-111_6655b612-f3b7-11eb-85b4-0800200c9a66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Almirall, LLC
- Application
- NDA021978
- Marketing category
- NDA
- Marketing start
- 2006-10-06
- Marketing end
- 0000-00-00
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 16110-111-00 | 16110011100 | 1 CAN in 1 CARTON (16110-111-00) > 100 g in 1 CAN | 1 can | 2016-10-01 | 0000-00-00 | No | No | Current |