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Desloratadine
Desloratadine - 0781-5226-01 - (Desloratadine)
Drug Information of Desloratadine
| Product NDC: | 0781-5226 |
| Proprietary Name: | Desloratadine |
| Non Proprietary Name: | Desloratadine |
| Active Ingredient(s): | 5 mg/1 & nbsp; Desloratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desloratadine
| Product NDC: | 0781-5226 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078364 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130701 |
Package Information of Desloratadine
| Package NDC: | 0781-5226-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0781-5226-01) |
NDC Information of Desloratadine
| NDC Code | 0781-5226-01 |
| Proprietary Name | Desloratadine |
| Package Description | 100 TABLET in 1 BOTTLE (0781-5226-01) |
| Product NDC | 0781-5226 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desloratadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | DESLORATADINE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
