NDC Code | 68084-286-01 |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-286-01) > 10 TABLET in 1 BLISTER PACK (68084-286-11) |
Product NDC | 68084-286 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Fexofenadine Hydrochloride |
Non-Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20091209 |
Marketing Category Name | ANDA |
Application Number | ANDA076502 |
Manufacturer | American Health Packaging |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength | 60 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |