Clobetasol Propionate
- Product NDC
- 50090-5778
- 11-digit product format
- 500905778
- Labeler code
- 50090
- Product ID
- 50090-5778_8ce776be-6cca-461a-9a85-9523f809abe1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209361
- Marketing category
- ANDA
- Marketing start
- 2017-11-04
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 0 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 |
|---|
| 50090-5778-0 | 50090577800 | 1 BOTTLE in 1 CARTON (50090-5778-0) > 50 mL in 1 BOTTLE | 1 bottle | 2021-10-07 | 0000-00-00 | No | No | Current |