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ZYRTEC-D
ZYRTEC-D - 50580-728-52 - (Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride)
Drug Information of ZYRTEC-D
| Product NDC: | 50580-728 |
| Proprietary Name: | ZYRTEC-D |
| Non Proprietary Name: | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZYRTEC-D
| Product NDC: | 50580-728 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021150 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080101 |
Package Information of ZYRTEC-D
| Package NDC: | 50580-728-52 |
| Package Description: | 24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of ZYRTEC-D
| NDC Code | 50580-728-52 |
| Proprietary Name | ZYRTEC-D |
| Package Description | 24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 50580-728 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080101 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
