CLOBETASOL PROPIONATE
- Product NDC
- 71589-018
- 11-digit product format
- 715890018
- Labeler code
- 71589
- Product ID
- 71589-018_c6c323a1-193c-428b-bded-8d7dde1adbb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLOBETASOL PROPIONATE
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA215838
- Marketing category
- ANDA
- Marketing start
- 2022-04-21
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-018-31 | 71589001831 | 1 CAN in 1 CARTON (71589-018-31) > 100 g in 1 CAN | 1 can | 2022-04-21 | 0000-00-00 | No | No | Current |
| 71589-018-50 | 71589001850 | 1 CAN in 1 CARTON (71589-018-50) > 50 g in 1 CAN | 1 can | 2022-04-21 | 0000-00-00 | No | No | Current |