| NDC Code | 50580-728-24 | 
|---|
			| Package Description | 4 BLISTER PACK in 1 CARTON (50580-728-24)  / 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] | 
|---|