| NDC Code | 72090-010-02 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (72090-010-02) |
|---|
| Product NDC | 72090-010 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20241003 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210137 |
|---|
| Manufacturer | Pioneer Life Sciences, LLC |
|---|
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
|---|
| Strength | 180 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|