NDC Code | 66715-9707-1 |
Package Description | 1 BLISTER PACK in 1 CARTON (66715-9707-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 66715-9707 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Allegra Allergy |
Non-Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20140901 |
Marketing Category Name | NDA |
Application Number | NDA020872 |
Manufacturer | Lil' Drug Store Products, Inc |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength | 180 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |