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Childrens Zyrtec Hives Relief
Childrens Zyrtec Hives Relief - 50580-731-05 - (Cetirizine Hydrochloride)
Drug Information of Childrens Zyrtec Hives Relief
| Product NDC: | 50580-731 |
| Proprietary Name: | Childrens Zyrtec Hives Relief |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Zyrtec Hives Relief
| Product NDC: | 50580-731 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022155 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of Childrens Zyrtec Hives Relief
| Package NDC: | 50580-731-05 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50580-731-05) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Information of Childrens Zyrtec Hives Relief
| NDC Code | 50580-731-05 |
| Proprietary Name | Childrens Zyrtec Hives Relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50580-731-05) > 118 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 50580-731 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
