| 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] |