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Clarinex
Clarinex - 0085-1334-01 - (Desloratadine)
Drug Information of Clarinex
| Product NDC: | 0085-1334 |
| Proprietary Name: | Clarinex |
| Non Proprietary Name: | Desloratadine |
| Active Ingredient(s): | .5 mg/mL & nbsp; Desloratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clarinex
| Product NDC: | 0085-1334 |
| Labeler Name: | Schering Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021300 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101222 |
Package Information of Clarinex
| Package NDC: | 0085-1334-01 |
| Package Description: | 473 mL in 1 BOTTLE (0085-1334-01) |
NDC Information of Clarinex
| NDC Code | 0085-1334-01 |
| Proprietary Name | Clarinex |
| Package Description | 473 mL in 1 BOTTLE (0085-1334-01) |
| Product NDC | 0085-1334 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desloratadine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20101222 |
| Marketing Category Name | NDA |
| Labeler Name | Schering Corporation |
| Substance Name | DESLORATADINE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
