OLUX
- Product NDC
- 0378-8182
- 11-digit product format
- 003788182
- Labeler code
- 0378
- Product ID
- 0378-8182_aa5310b2-f624-4ac5-bc4a-c907a505d65a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clobetasol propionate
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- NDA021142
- Marketing category
- NDA
- Marketing start
- 2018-12-11
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0378-8182-01 | 00378818201 | 100 g in 1 CAN (0378-8182-01) | 100 g | 2018-12-17 | 0000-00-00 | No | No | Current |
| 0378-8182-06 | 00378818206 | 12 g in 1 CAN (0378-8182-06) | 12 g | 2018-12-17 | 0000-00-00 | Yes | No | Current |
| 0378-8182-50 | 00378818250 | 50 g in 1 CAN (0378-8182-50) | 50 g | 2019-04-11 | 0000-00-00 | No | No | Current |