Product NDC: | 21695-815 |
Proprietary Name: | Clarinex |
Non Proprietary Name: | Desloratadine |
Active Ingredient(s): | 5 mg/1 & nbsp; Desloratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-815 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021297 |
Marketing Category: | NDA |
Start Marketing Date: | 20020208 |
Package NDC: | 21695-815-10 |
Package Description: | 10 TABLET, FILM COATED in 1 BOTTLE (21695-815-10) |
NDC Code | 21695-815-10 |
Proprietary Name | Clarinex |
Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (21695-815-10) |
Product NDC | 21695-815 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Desloratadine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20020208 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | DESLORATADINE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |