| NDC Code | 55289-957-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-957-90) |
|---|
| Product NDC | 55289-957 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100521 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077081 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 180 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
|---|