Desonide
- Product NDC
- 46708-485
- 11-digit product format
- 467080485
- Labeler code
- 46708
- Product ID
- 46708-485_98a69c58-33de-41e1-a26f-7a4152605f05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA212473
- Marketing category
- ANDA
- Marketing start
- 2025-03-07
- Substance
- DESONIDE
- Active strength
- .5 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 46708-485-15 | 46708048515 | 1 TUBE in 1 CARTON (46708-485-15) / 15 g in 1 TUBE | 1 tube | 2025-03-07 | No | No | Historical |
| 46708-485-60 | 46708048560 | 1 TUBE in 1 CARTON (46708-485-60) / 60 g in 1 TUBE | 1 tube | 2025-03-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Desonide Ointment, 0.05% | Alembic Pharmaceuticals Limited | 2025-03-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |