Home
>
National Drug Code (NDC)
>
CLARINEX-D 24 HOUR
CLARINEX-D 24 HOUR - 0085-1317-01 - (desloratadine and pseudoephedrine sulfate)
Drug Information of CLARINEX-D 24 HOUR
| Product NDC: | 0085-1317 |
| Proprietary Name: | CLARINEX-D 24 HOUR |
| Non Proprietary Name: | desloratadine and pseudoephedrine sulfate |
| Active Ingredient(s): | 5; 240 mg/1; mg/1 & nbsp; desloratadine and pseudoephedrine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLARINEX-D 24 HOUR
| Product NDC: | 0085-1317 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021605 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050303 |
Package Information of CLARINEX-D 24 HOUR
| Package NDC: | 0085-1317-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0085-1317-01) |
NDC Information of CLARINEX-D 24 HOUR
| NDC Code | 0085-1317-01 |
| Proprietary Name | CLARINEX-D 24 HOUR |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0085-1317-01) |
| Product NDC | 0085-1317 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desloratadine and pseudoephedrine sulfate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20050303 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | DESLORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 5; 240 |
| 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] |
