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Alcortin
Alcortin - 68040-702-13 - (1% iodoquinol - 2% hydrocortisone)
Drug Information of Alcortin
| Product NDC: | 68040-702 |
| Proprietary Name: | Alcortin |
| Non Proprietary Name: | 1% iodoquinol - 2% hydrocortisone |
| Active Ingredient(s): | 2; 1 g/100g; g/100g & nbsp; 1% iodoquinol - 2% hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alcortin
| Product NDC: | 68040-702 |
| Labeler Name: | Primus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20030725 |
Package Information of Alcortin
| Package NDC: | 68040-702-13 |
| Package Description: | 12 CARTON in 1 BOX (68040-702-13) > 24 PACKET in 1 CARTON > 2 g in 1 PACKET |
NDC Information of Alcortin
| NDC Code | 68040-702-13 |
| Proprietary Name | Alcortin |
| Package Description | 12 CARTON in 1 BOX (68040-702-13) > 24 PACKET in 1 CARTON > 2 g in 1 PACKET |
| Product NDC | 68040-702 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | 1% iodoquinol - 2% hydrocortisone |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20030725 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Primus Pharmaceuticals |
| Substance Name | HYDROCORTISONE; IODOQUINOL |
| Strength Number | 2; 1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
