Clobetasol Propionate
- Product NDC
- 50436-9985
- 11-digit product format
- 504369985
- Labeler code
- 50436
- Product ID
- 50436-9985_f8817f00-6617-44a5-9853-9a49d848ed69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clobetasol propionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Unit Dose Services
- Application
- ANDA074392
- Marketing category
- ANDA
- Marketing start
- 1996-09-30
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-9985-1 | Clobetasol Propionate | 45 g in 1 TUBE | CREAM | 45 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-9985 | CLOBETASOL PROPIONATE CREAM [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20170312_c5f0a0f3-5852-49d4-ae34-7ae8feaf1a6e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50436-9985-1 | 50436998501 | 45 g in 1 TUBE | 45 g | Historical |