Product NDC: | 10337-550 |
Proprietary Name: | Carmol HC |
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) |
Product NDC: | 10337-550 |
Labeler Name: | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080505 |
Marketing Category: | ANDA |
Start Marketing Date: | 19730112 |
Package NDC: | 10337-550-19 |
Package Description: | 1 TUBE in 1 CARTON (10337-550-19) > 85 g in 1 TUBE |
NDC Code | 10337-550-19 |
Proprietary Name | Carmol HC |
Package Description | 1 TUBE in 1 CARTON (10337-550-19) > 85 g in 1 TUBE |
Product NDC | 10337-550 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydrocortisone acetate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19730112 |
Marketing Category Name | ANDA |
Labeler Name | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
Substance Name | HYDROCORTISONE ACETATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |