Desonide
- Product NDC
- 72162-2005
- 11-digit product format
- 721622005
- Labeler code
- 72162
- Product ID
- 72162-2005_a0792f7b-faeb-475d-a030-ef46e876c2d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210198
- Marketing category
- ANDA
- Marketing start
- 2020-06-17
- Substance
- DESONIDE
- Active strength
- .5 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| J280872D1O | DESONIDE | 638-94-8 | DESONIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2005-2 | 72162200502 | 1 TUBE in 1 CARTON (72162-2005-2) / 15 g in 1 TUBE | 1 tube | 2020-06-17 | No | No | Historical |
| 72162-2005-6 | 72162200506 | 1 TUBE in 1 CARTON (72162-2005-6) / 60 g in 1 TUBE | 1 tube | 2020-06-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Desonide Cream USP, 0.05% | Bryant Ranch Prepack | 2026-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 101 |