Product NDC: | 59762-0074 |
Proprietary Name: | Hydrocortisone |
Non Proprietary Name: | HYDROCORTISONE |
Active Ingredient(s): | 10 mg/1 & nbsp; HYDROCORTISONE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59762-0074 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA008697 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20121219 |
Package NDC: | 59762-0074-1 |
Package Description: | 100 TABLET in 1 BOTTLE (59762-0074-1) |
NDC Code | 59762-0074-1 |
Proprietary Name | Hydrocortisone |
Package Description | 100 TABLET in 1 BOTTLE (59762-0074-1) |
Product NDC | 59762-0074 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROCORTISONE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121219 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Greenstone LLC |
Substance Name | HYDROCORTISONE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |