Clobetasol Propionate
- Product NDC
- 72162-1438
- 11-digit product format
- 721621438
- Labeler code
- 72162
- Product ID
- 72162-1438_beb3d6d1-d7c3-4726-93fc-54cb0aea1665
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol propionate
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075027
- Marketing category
- ANDA
- Marketing start
- 2008-07-30
- 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 |
|---|
| 72162-1438-2 | 72162143802 | 1 TUBE in 1 CARTON (72162-1438-2) / 15 g in 1 TUBE | 1 tube | 2023-08-16 | No | No | Historical |
| 72162-1438-3 | 72162143803 | 1 TUBE in 1 CARTON (72162-1438-3) / 30 g in 1 TUBE | 1 tube | 2023-08-16 | No | No | Historical |
| 72162-1438-6 | 72162143806 | 1 TUBE in 1 CARTON (72162-1438-6) / 60 g in 1 TUBE | 1 tube | 2023-08-16 | No | No | Historical |