NDC Code |
21695-820-14 |
Proprietary Name |
FEXOFENADINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
Package Description |
14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-820-14) |
Product NDC |
21695-820 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
FEXOFENADINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
Dosage Form Name |
TABLET, FILM COATED, EXTENDED RELEASE |
Route Name |
ORAL |
Start Marketing Date |
20091102 |
Marketing Category Name |
NDA |
Labeler Name |
Rebel Distributors Corp |
Substance Name |
FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number |
60; 120 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |