Clobetasol Propionate
- Product NDC
- 71589-003
- 11-digit product format
- 715890003
- Labeler code
- 71589
- Product ID
- 71589-003_bdc0953a-d9e9-4766-b5fb-d7fe818b837b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA211191
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 0 g/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 71589-003-12 | 71589000312 | 1 BOTTLE in 1 CARTON (71589-003-12) > 125 mL in 1 BOTTLE | 1 bottle | 2019-10-31 | 0000-00-00 | No | No | Current |
| 71589-003-59 | 71589000359 | 1 BOTTLE in 1 CARTON (71589-003-59) > 59 mL in 1 BOTTLE | 1 bottle | 2019-10-31 | 0000-00-00 | No | No | Current |