desoximetasone
- Product NDC
- 72162-1427
- 11-digit product format
- 721621427
- Labeler code
- 72162
- Product ID
- 72162-1427_919757de-a723-4d2c-a397-b5e428ebebd3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desoximetasone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206441
- Marketing category
- ANDA
- Marketing start
- 2018-12-06
- Substance
- DESOXIMETASONE
- Active strength
- 2.5 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 |
|---|
| 4E07GXB7AU | DESOXIMETASONE | 382-67-2 | DESOXIMETASONE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1427-1 | 72162142701 | 1 BOTTLE, SPRAY in 1 CARTON (72162-1427-1) / 100 mL in 1 BOTTLE, SPRAY | 2024-12-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| desoximetasone | Bryant Ranch Prepack | 2024-12-24 | HUMAN PRESCRIPTION DRUG LABEL | 100 |