| NDC Code | 0378-0782-93 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0782-93) |
|---|
| Product NDC | 0378-0782 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110825 |
|---|
| End Marketing Date | 20220228 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077081 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 180 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|