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Proctocort
Proctocort - 65649-501-30 - (HYDROCORTISONE)
Drug Information of Proctocort
| Product NDC: | 65649-501 |
| Proprietary Name: | Proctocort |
| 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 Proctocort
| Product NDC: | 65649-501 |
| Labeler Name: | Salix Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20040601 |
Package Information of Proctocort
| Package NDC: | 65649-501-30 |
| Package Description: | 1 TUBE in 1 CARTON (65649-501-30) > 28.35 g in 1 TUBE |
NDC Information of Proctocort
| NDC Code | 65649-501-30 |
| Proprietary Name | Proctocort |
| Package Description | 1 TUBE in 1 CARTON (65649-501-30) > 28.35 g in 1 TUBE |
| Product NDC | 65649-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20040601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Salix Pharmaceuticals, Inc |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
