Product NDC: | 43478-270 |
Proprietary Name: | Hydrocortisone Butyrate |
Non Proprietary Name: | hydrocortisone butyrate |
Active Ingredient(s): | 1 mg/g & nbsp; hydrocortisone butyrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43478-270 |
Labeler Name: | Rouses Point Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018514 |
Marketing Category: | NDA |
Start Marketing Date: | 20090901 |
Package NDC: | 43478-270-45 |
Package Description: | 1 TUBE in 1 CARTON (43478-270-45) > 45 g in 1 TUBE |
NDC Code | 43478-270-45 |
Proprietary Name | Hydrocortisone Butyrate |
Package Description | 1 TUBE in 1 CARTON (43478-270-45) > 45 g in 1 TUBE |
Product NDC | 43478-270 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydrocortisone butyrate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20090901 |
Marketing Category Name | NDA |
Labeler Name | Rouses Point Pharmaceuticals, LLC |
Substance Name | HYDROCORTISONE BUTYRATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |