ALLEGRA - fexofenadine hydrochloride
Navigation: NDC > Supplier starting with: S > SANOFI AVENTIS U.S. LLC| Field | Value |
|---|---|
| NDC Code: | 0088-1097 |
| Proprietary Name: | ALLEGRA |
| Suffix: | |
| Non-Proprietary Name: | fexofenadine hydrochloride |
| Dosage Form: | SUSPENSION |
| Method: | ORAL |
| Original Marketing Date: | 16-10-2006 |
| Category Name: | NDA |
| Application Number: | NDA021963 |
| Labeler: | SANOFI AVENTIS U.S. LLC |
| Substance Name: | FEXOFENADINE HYDROCHLORIDE |
| Active Numerator Strength: | 6 |
| Active Ingredient Unit: | mg/mL |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |