Fexofenadine Hydrochloride - fexofenadine hydrochloride
Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 51079-529 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | fexofenadine hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 15-10-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA077081 |
| Labeler: | UDL LABORATORIES, INC. |
| Substance Name: | FEXOFENADINE HYDROCHLORIDE |
| Active Numerator Strength: | 60 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |