DESONATE
- Product NDC
- 50222-504
- 11-digit product format
- 502220504
- Labeler code
- 50222
- Product ID
- 50222-504_aa3a2f30-fe57-4537-a459-096fa514e7c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- LEO Pharma Inc.
- Application
- NDA021844
- Marketing category
- NDA
- Marketing start
- 2018-10-01
- 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 |
|---|
| 50222-504-60 | 50222050460 | 1 TUBE in 1 CARTON (50222-504-60) > 60 g in 1 TUBE | 1 tube | 2018-10-01 | 0000-00-00 | No | No | Current |
| 50222-504-91 | 50222050491 | 1 TUBE in 1 CARTON (50222-504-91) > 3.5 g in 1 TUBE | 1 tube | 2018-10-01 | 0000-00-00 | No | No | Current |