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Hydrocortisone
Hydrocortisone - 59762-0075-1 - (HYDROCORTISONE)
Drug Information of Hydrocortisone
| Product NDC: | 59762-0075 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | HYDROCORTISONE |
| Active Ingredient(s): | 20 mg/1 & nbsp; HYDROCORTISONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 59762-0075 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA008697 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121219 |
Package Information of Hydrocortisone
| Package NDC: | 59762-0075-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (59762-0075-1) |
NDC Information of Hydrocortisone
| NDC Code | 59762-0075-1 |
| Proprietary Name | Hydrocortisone |
| Package Description | 100 TABLET in 1 BOTTLE (59762-0075-1) |
| Product NDC | 59762-0075 |
| 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 | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
