Clobetasol Propionate
- Product NDC
- 71335-2851
- 11-digit product format
- 713352851
- Labeler code
- 71335
- Product ID
- 71335-2851_4db5a23c-74bd-4c6f-8520-af56a726e432
- 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Clobetasol Propionate
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| CLOBETASOL PROPIONATE | .5 mg/g |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 779619577M |
| Rxcui | 861448 |
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 |
|---|
| 71335-2851-1 | 71335285101 | 1 TUBE in 1 CARTON (71335-2851-1) / 15 g in 1 TUBE | 1 tube | 2025-10-22 | No | No | Historical |