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LEADER ALL DAY ALLERGY
LEADER ALL DAY ALLERGY - 37205-820-65 - (cetirizine)
Drug Information of LEADER ALL DAY ALLERGY
| Product NDC: | 37205-820 |
| Proprietary Name: | LEADER ALL DAY ALLERGY |
| Non Proprietary Name: | cetirizine |
| Active Ingredient(s): | 10 mg/1 & nbsp; cetirizine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEADER ALL DAY ALLERGY
| Product NDC: | 37205-820 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077498 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071227 |
Package Information of LEADER ALL DAY ALLERGY
| Package NDC: | 37205-820-65 |
| Package Description: | 30 TABLET in 1 BOTTLE (37205-820-65) |
NDC Information of LEADER ALL DAY ALLERGY
| NDC Code | 37205-820-65 |
| Proprietary Name | LEADER ALL DAY ALLERGY |
| Package Description | 30 TABLET in 1 BOTTLE (37205-820-65) |
| Product NDC | 37205-820 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | cetirizine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071227 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
