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Hydrocortisone
Hydrocortisone - 68788-9922-2 - (Hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 68788-9922 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 25 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 68788-9922 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085025 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120127 |
Package Information of Hydrocortisone
| Package NDC: | 68788-9922-2 |
| Package Description: | 1 TUBE in 1 CARTON (68788-9922-2) > 28 g in 1 TUBE |
NDC Information of Hydrocortisone
| NDC Code | 68788-9922-2 |
| Proprietary Name | Hydrocortisone |
| Package Description | 1 TUBE in 1 CARTON (68788-9922-2) > 28 g in 1 TUBE |
| Product NDC | 68788-9922 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120127 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | HYDROCORTISONE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
