Clobetasol Propionate
- Product NDC
- 50742-304
- 11-digit product format
- 507420304
- Labeler code
- 50742
- Product ID
- 50742-304_7e74be38-4742-4560-b0e9-7e9be5de1afd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA206805
- Marketing category
- ANDA
- Marketing start
- 2017-07-31
- Marketing end
- 2023-07-31
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-304-01 | 50742030401 | 1 CAN in 1 CARTON (50742-304-01) > 100 g in 1 CAN | 1 can | 2017-07-31 | 0000-00-00 | No | No | Current |
| 50742-304-50 | 50742030450 | 1 CAN in 1 CARTON (50742-304-50) > 50 g in 1 CAN | 1 can | 2017-07-31 | 0000-00-00 | No | No | Current |