NDC Code |
0555-0725-08 |
Proprietary Name |
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
Package Description |
19635 TABLET, MULTILAYER, EXTENDED RELEASE in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (0555-0725-08) |
Product NDC |
0555-0725 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
Dosage Form Name |
TABLET, MULTILAYER, EXTENDED RELEASE |
Route Name |
ORAL |
Start Marketing Date |
20110211 |
Marketing Category Name |
ANDA |
Labeler Name |
Barr Laboratories Inc. |
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] |