Product NDC: | 45802-472 |
Proprietary Name: | Hydrocortisone Acetate Pramoxine Hcl |
Non Proprietary Name: | Hydrocortisone Acetate Pramoxine Hcl |
Active Ingredient(s): | 2.5; 1 g/100g; g/100g & nbsp; Hydrocortisone Acetate Pramoxine Hcl |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45802-472 |
Labeler Name: | Perrigo New York Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19960927 |
Package NDC: | 45802-472-64 |
Package Description: | 1 TUBE in 1 CARTON (45802-472-64) > 28.35 g in 1 TUBE |
NDC Code | 45802-472-64 |
Proprietary Name | Hydrocortisone Acetate Pramoxine Hcl |
Package Description | 1 TUBE in 1 CARTON (45802-472-64) > 28.35 g in 1 TUBE |
Product NDC | 45802-472 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrocortisone Acetate Pramoxine Hcl |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19960927 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Perrigo New York Inc |
Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
Strength Number | 2.5; 1 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |