Clobetasol Propionate
- Product NDC
- 71589-004
- 11-digit product format
- 715890004
- Labeler code
- 71589
- Product ID
- 71589-004_6d4955ce-e763-4878-8d8f-716e45561500
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA212881
- Marketing category
- ANDA
- Marketing start
- 2019-11-02
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/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 |
|---|
| 71589-004-25 | 71589000425 | 1 BOTTLE in 1 CARTON (71589-004-25) > 25 mL in 1 BOTTLE | 1 bottle | 2019-11-02 | 0000-00-00 | No | No | Current |
| 71589-004-50 | 71589000450 | 1 BOTTLE in 1 CARTON (71589-004-50) > 50 mL in 1 BOTTLE | 1 bottle | 2019-11-02 | 0000-00-00 | No | No | Current |