NDC Code | 72090-010-99 |
Package Description | 1000 TABLET in 1 BOTTLE (72090-010-99) |
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 | 20230811 |
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] |