Halobetasol Propionate
- Product NDC
- 63629-8735
- 11-digit product format
- 636298735
- Labeler code
- 63629
- Product ID
- 63629-8735_60f1cc87-3501-49d7-8ef4-4d1860d88682
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- halobetasol propionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077001
- Marketing category
- ANDA
- Marketing start
- 2004-12-16
- Marketing end
- 0000-00-00
- Substance
- HALOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 91A0K1TY3Z | HALOBETASOL PROPIONATE | 66852-54-8 | HALOBETASOL PROPIONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8735-1 | 63629873501 | 15 g in 1 TUBE (63629-8735-1) | 15 g | 2021-08-19 | 0000-00-00 | No | No | Current |