NDC Code | 51316-018-15 |
Package Description | 3 BLISTER PACK in 1 CARTON (51316-018-15) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 51316-018 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
Non-Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20221130 |
Marketing Category Name | ANDA |
Application Number | ANDA079043 |
Manufacturer | CVS Pharmacy, Inc |
Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 180; 240 |
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] |