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Hydrocortisone
Hydrocortisone - 0603-0535-50 - (hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 0603-0535 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 0603-0535 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20011001 |
Package Information of Hydrocortisone
| Package NDC: | 0603-0535-50 |
| Package Description: | 1 TUBE in 1 CARTON (0603-0535-50) > 28.4 g in 1 TUBE |
NDC Information of Hydrocortisone
| NDC Code | 0603-0535-50 |
| Proprietary Name | Hydrocortisone |
| Package Description | 1 TUBE in 1 CARTON (0603-0535-50) > 28.4 g in 1 TUBE |
| Product NDC | 0603-0535 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20011001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
