Desonide
- Product NDC
- 46708-550
- 11-digit product format
- 467080550
- Labeler code
- 46708
- Product ID
- 46708-550_07cc1eb5-c405-4e18-a83a-fd8bb6864ca9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA213632
- Marketing category
- ANDA
- Marketing start
- 2025-03-26
- Substance
- DESONIDE
- Active strength
- .5 mg/mL
- 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 |
|---|
| 46708-550-18 | 46708055018 | 1 BOTTLE in 1 CARTON (46708-550-18) / 118 mL in 1 BOTTLE | 1 bottle | 2025-03-26 | No | No | Historical |
| 46708-550-59 | 46708055059 | 1 BOTTLE in 1 CARTON (46708-550-59) / 59 mL in 1 BOTTLE | 1 bottle | 2025-03-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Desonide | Alembic Pharmaceuticals Limited | 2025-03-26 | HUMAN PRESCRIPTION DRUG LABEL | 1 |