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U-Cort
U-Cort - 51672-3009-2 - (Hydrocortisone Acetate)
Drug Information of U-Cort
| Product NDC: | 51672-3009 |
| Proprietary Name: | U-Cort |
| Non Proprietary Name: | Hydrocortisone Acetate |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of U-Cort
| Product NDC: | 51672-3009 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089472 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880613 |
Package Information of U-Cort
| Package NDC: | 51672-3009-2 |
| Package Description: | 1 TUBE in 1 CARTON (51672-3009-2) > 28.35 g in 1 TUBE |
NDC Information of U-Cort
| NDC Code | 51672-3009-2 |
| Proprietary Name | U-Cort |
| Package Description | 1 TUBE in 1 CARTON (51672-3009-2) > 28.35 g in 1 TUBE |
| Product NDC | 51672-3009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19880613 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
