Product NDC: | 16590-121 |
Proprietary Name: | HYDROCORTISONE |
Non Proprietary Name: | HYDROCORTISONE |
Active Ingredient(s): | 10 mg/g & nbsp; HYDROCORTISONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-121 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087795 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020103 |
Package NDC: | 16590-121-30 |
Package Description: | 1 TUBE in 1 CARTON (16590-121-30) > 28.4 g in 1 TUBE |
NDC Code | 16590-121-30 |
Proprietary Name | HYDROCORTISONE |
Package Description | 1 TUBE in 1 CARTON (16590-121-30) > 28.4 g in 1 TUBE |
Product NDC | 16590-121 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROCORTISONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20020103 |
Marketing Category Name | ANDA |
Labeler Name | STAT Rx USA LLC |
Substance Name | HYDROCORTISONE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |