| NDC Code | 51316-007-84 |
|---|
| Package Description | 3 BLISTER PACK in 1 CARTON (51316-007-84) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 51316-007 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride |
|---|
| Non-Proprietary Name | Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20221117 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209116 |
|---|
| Manufacturer | CVS Pharmacy, Inc. |
|---|
| 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] |
|---|