Product NDC: | 62011-0093 |
Proprietary Name: | Childrens Cetirizine Hydrochloride |
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: | 62011-0093 |
Labeler Name: | Health Mart |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA201546 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110520 |
Package NDC: | 62011-0093-1 |
Package Description: | 1 BOTTLE in 1 CARTON (62011-0093-1) > 118 mL in 1 BOTTLE |
NDC Code | 62011-0093-1 |
Proprietary Name | Childrens Cetirizine Hydrochloride |
Package Description | 1 BOTTLE in 1 CARTON (62011-0093-1) > 118 mL in 1 BOTTLE |
Product NDC | 62011-0093 |
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 | Health Mart |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes |