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Clarinex-D 12 Hour
Clarinex-D 12 Hour - 54868-5708-1 - (desloratadine and pseudoephedrine sulfate)
Drug Information of Clarinex-D 12 Hour
| Product NDC: | 54868-5708 |
| Proprietary Name: | Clarinex-D 12 Hour |
| Non Proprietary Name: | desloratadine and pseudoephedrine sulfate |
| Active Ingredient(s): | 2.5; 120 mg/1; mg/1 & nbsp; desloratadine and pseudoephedrine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clarinex-D 12 Hour
| Product NDC: | 54868-5708 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021313 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20061129 |
Package Information of Clarinex-D 12 Hour
| Package NDC: | 54868-5708-1 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5708-1) |
NDC Information of Clarinex-D 12 Hour
| NDC Code | 54868-5708-1 |
| Proprietary Name | Clarinex-D 12 Hour |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5708-1) |
| Product NDC | 54868-5708 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desloratadine and pseudoephedrine sulfate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20061129 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DESLORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 2.5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
