Product NDC: | 15014-185 |
Proprietary Name: | NuCort |
Non Proprietary Name: | Hydrocortisone Acetate |
Active Ingredient(s): | 20 mg/g & nbsp; Hydrocortisone Acetate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 15014-185 |
Labeler Name: | Gentex Pharma |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100816 |
Package NDC: | 15014-185-02 |
Package Description: | 1 BOTTLE in 1 CARTON (15014-185-02) > 56.7 g in 1 BOTTLE |
NDC Code | 15014-185-02 |
Proprietary Name | NuCort |
Package Description | 1 BOTTLE in 1 CARTON (15014-185-02) > 56.7 g in 1 BOTTLE |
Product NDC | 15014-185 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrocortisone Acetate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100816 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Gentex Pharma |
Substance Name | HYDROCORTISONE ACETATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |