| Product NDC: | 37205-591 |
| Proprietary Name: | Leader Childrens Allergy Relief |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37205-591 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA201546 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110520 |
| Package NDC: | 37205-591-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (37205-591-26) > 120 mL in 1 BOTTLE |
| NDC Code | 37205-591-26 |
| Proprietary Name | Leader Childrens Allergy Relief |
| Package Description | 1 BOTTLE in 1 CARTON (37205-591-26) > 120 mL in 1 BOTTLE |
| Product NDC | 37205-591 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110520 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |