| NDC Code | 57483-240-02 |
|---|
| Package Description | 150 TABLET in 1 CONTAINER (57483-240-02) |
|---|
| Product NDC | 57483-240 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Crcle Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20201218 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211075 |
|---|
| Manufacturer | Innovus Pharmaceuticals, Inc. |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 180 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|