FEXOFENADINE HYDROCHLORIDE - FEXOFENADINE HYDROCHLORIDE
Navigation: NDC > Supplier starting with: S > SUN PHARMACEUTICAL INDUSTRIES LIMITED| Field | Value |
|---|---|
| NDC Code: | 62756-543 |
| Proprietary Name: | FEXOFENADINE HYDROCHLORIDE |
| Suffix: | |
| Non-Proprietary Name: | FEXOFENADINE HYDROCHLORIDE |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 06-02-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA091567 |
| Labeler: | SUN PHARMACEUTICAL INDUSTRIES LIMITED |
| Substance Name: | FEXOFENADINE HYDROCHLORIDE |
| Active Numerator Strength: | 60 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |