NDC Code | 0363-1606-20 |
Package Description | 4 BLISTER PACK in 1 CARTON (0363-1606-20) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 0363-1606 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hci |
Non-Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hci |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20190916 |
Marketing Category Name | ANDA |
Application Number | ANDA076667 |
Manufacturer | Walgreens Company |
Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 60; 120 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC] |