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NDC 50090-5979-00 Clobetasol Propionate Cream USP, 0.05% 0.5 mg/g Details
Clobetasol Propionate Cream USP, 0.05% 0.5 mg/g
Clobetasol Propionate Cream USP, 0.05% is a TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is CLOBETASOL PROPIONATE.
MedlinePlus Drug Summary
Clobetasol topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various scalp and skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body) and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Clobetasol is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
Related Packages: 50090-5979-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clobetasol Topical
Product Information
| NDC | 50090-5979 |
|---|---|
| Product ID | 50090-5979_b7f86f9d-4521-4b49-90d3-0c4d273f9f8a |
| Associated GPIs | 90550025103705 |
| GCN Sequence Number | 007634 |
| GCN Sequence Number Description | clobetasol propionate CREAM (G) 0.05 % TOPICAL |
| HIC3 | Q5P |
| HIC3 Description | TOPICAL ANTI-INFLAMMATORY STEROIDAL |
| GCN | 32140 |
| HICL Sequence Number | 003327 |
| HICL Sequence Number Description | CLOBETASOL PROPIONATE |
| Brand/Generic | Generic |
| Proprietary Name | Clobetasol Propionate Cream USP, 0.05% |
| Proprietary Name Suffix | Clobetasol Propionate Cream USP, 0.05% |
| Non-Proprietary Name | Clobetasol Propionate USP, 0.05% |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 0.5 |
| Active Ingredient Units | mg/g |
| Substance Name | CLOBETASOL PROPIONATE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA212982 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-5979-00 (50090597900)
| NDC Package Code | 50090-5979-0 |
|---|---|
| Billing NDC | 50090597900 |
| Package | 30 g in 1 TUBE (50090-5979-0) |
| Marketing Start Date | 2022-05-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |