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NuCort
NuCort - 15014-185-02 - (Hydrocortisone Acetate)
Drug Information of NuCort
| 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) |
Labeler Information of NuCort
| 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 Information of NuCort
| Package NDC: | 15014-185-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (15014-185-02) > 56.7 g in 1 BOTTLE |
NDC Information of NuCort
| 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] |
