| 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] |