Clobetasol Propionate
- Product NDC
- 71335-2860
- 11-digit product format
- 713352860
- Labeler code
- 71335
- Product ID
- 71335-2860_f411c096-9074-4dde-8e1a-76ee2bd0361a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate Ointment USP, 0.05%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211295
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Substance
- CLOBETASOL PROPIONATE
- 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 |
|---|
| 779619577M | CLOBETASOL PROPIONATE | 25122-46-7 | CLOBETASOL PROPIONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2860-1 | 71335286001 | 1 TUBE in 1 CARTON (71335-2860-1) / 30 g in 1 TUBE | 1 tube | 2025-10-22 | No | No | Historical |