NDC Code | 68071-5191-3 |
Package Description | 30 TABLET in 1 BOTTLE (68071-5191-3) |
Product NDC | 68071-5191 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Fexofenadine Hydrochloride |
Non-Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20110103 |
Marketing Category Name | ANDA |
Application Number | ANDA076502 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength | 180 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |