Desloratadine - Desloratadine
Navigation: NDC > Supplier starting with: N > NORTHSTAR RX LLC| Field | Value |
|---|---|
| NDC Code: | 16714-339 |
| Proprietary Name: | Desloratadine |
| Suffix: | |
| Non-Proprietary Name: | Desloratadine |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 16-01-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA078357 |
| Labeler: | NORTHSTAR RX LLC |
| Substance Name: | DESLORATADINE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |