Product NDC: | 68220-140 |
Proprietary Name: | Cortifoam |
Non Proprietary Name: | hydrocortisone acetate |
Active Ingredient(s): | 1500 mg/15g & nbsp; hydrocortisone acetate |
Administration Route(s): | RECTAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68220-140 |
Labeler Name: | Alaven Pharmaceutical LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017351 |
Marketing Category: | NDA |
Start Marketing Date: | 19820212 |
Package NDC: | 68220-140-15 |
Package Description: | 1 CONTAINER in 1 CARTON (68220-140-15) > 15 g in 1 CONTAINER |
NDC Code | 68220-140-15 |
Proprietary Name | Cortifoam |
Package Description | 1 CONTAINER in 1 CARTON (68220-140-15) > 15 g in 1 CONTAINER |
Product NDC | 68220-140 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydrocortisone acetate |
Dosage Form Name | AEROSOL, FOAM |
Route Name | RECTAL |
Start Marketing Date | 19820212 |
Marketing Category Name | NDA |
Labeler Name | Alaven Pharmaceutical LLC |
Substance Name | HYDROCORTISONE ACETATE |
Strength Number | 1500 |
Strength Unit | mg/15g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |