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Hydrocortisone
Hydrocortisone - 0574-0420-25 - (Hydrocortisone)
Drug Information of Hydrocortisone
| 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) |
Labeler Information of Hydrocortisone
| 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 Information of Hydrocortisone
| Package NDC: | 0574-0420-25 |
| Package Description: | 25 g in 1 BOTTLE (0574-0420-25) |
NDC Information of Hydrocortisone
| NDC Code | 0574-0420-25 |
| Proprietary Name | Hydrocortisone |
| Package Description | 25 g in 1 BOTTLE (0574-0420-25) |
| 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] |
