Fexofenadine Hydrochloride - Fexofenadine Hydrochloride
Navigation: NDC > Supplier starting with: T > TEVA PHARMACEUTICAL INDUSTRIES LTD.| Field | Value |
|---|---|
| NDC Code: | 0480-7251 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Fexofenadine Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 17-09-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA076447 |
| Labeler: | TEVA PHARMACEUTICAL INDUSTRIES LTD. |
| Substance Name: | FEXOFENADINE HYDROCHLORIDE |
| Active Numerator Strength: | 30 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule: |