Product NDC: | 37205-826 |
Proprietary Name: | Childrens All Day Allergy |
Non Proprietary Name: | cetirizine hydrochloride |
Active Ingredient(s): | 5 mg/5mL & nbsp; cetirizine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-826 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA090254 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090929 |
Package NDC: | 37205-826-26 |
Package Description: | 1 BOTTLE in 1 CARTON (37205-826-26) > 120 mL in 1 BOTTLE |
NDC Code | 37205-826-26 |
Proprietary Name | Childrens All Day Allergy |
Package Description | 1 BOTTLE in 1 CARTON (37205-826-26) > 120 mL in 1 BOTTLE |
Product NDC | 37205-826 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | cetirizine hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090929 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |