Product NDC: | 0574-0420 |
Proprietary Name: | Hydrocortisone |
Non Proprietary Name: | Hydrocortisone |
Active Ingredient(s): | 1 g/g & nbsp; Hydrocortisone |
Administration Route(s): | NOT APPLICABLE |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0574-0420 |
Labeler Name: | Paddock Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 19830408 |
Package NDC: | 0574-0420-01 |
Package Description: | 100 g in 1 BOTTLE (0574-0420-01) |
NDC Code | 0574-0420-01 |
Proprietary Name | Hydrocortisone |
Package Description | 100 g in 1 BOTTLE (0574-0420-01) |
Product NDC | 0574-0420 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrocortisone |
Dosage Form Name | POWDER |
Route Name | NOT APPLICABLE |
Start Marketing Date | 19830408 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | Paddock Laboratories, Inc. |
Substance Name | HYDROCORTISONE |
Strength Number | 1 |
Strength Unit | g/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |