NDC Code | 70518-1218-2 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1218-2) |
Product NDC | 70518-1218 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Fexofenadine Hydrochloride |
Non-Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20180518 |
Marketing Category Name | ANDA |
Application Number | ANDA202039 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength | 180 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |