| NDC Code | 50580-728-25 |
|---|
| Package Description | 4 BLISTER PACK in 1 CARTON (50580-728-25) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 50580-728 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Zyrtec-d |
|---|
| Proprietary Name Suffix | Allergy Plus Congestion |
|---|
| Non-Proprietary Name | Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20080101 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021150 |
|---|
| Manufacturer | Kenvue Brands LLC |
|---|
| Substance Name | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
|---|
| Strength | 5; 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] |
|---|