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Cordran
Cordran - 16110-034-30 - (Flurandrenolide)
Drug Information of Cordran
| Product NDC: | 16110-034 |
| Proprietary Name: | Cordran |
| Non Proprietary Name: | Flurandrenolide |
| Active Ingredient(s): | .25 mg/g & nbsp; Flurandrenolide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cordran
| Product NDC: | 16110-034 |
| Labeler Name: | Aqua Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012806 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19651018 |
Package Information of Cordran
| Package NDC: | 16110-034-30 |
| Package Description: | 30 g in 1 TUBE (16110-034-30) |
NDC Information of Cordran
| NDC Code | 16110-034-30 |
| Proprietary Name | Cordran |
| Package Description | 30 g in 1 TUBE (16110-034-30) |
| Product NDC | 16110-034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flurandrenolide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19651018 |
| Marketing Category Name | NDA |
| Labeler Name | Aqua Pharmaceuticals, LLC |
| Substance Name | FLURANDRENOLIDE |
| Strength Number | .25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
