Product NDC: | 11822-0974 |
Proprietary Name: | childrens allergy relief |
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: | 11822-0974 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA090254 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080417 |
Package NDC: | 11822-0974-1 |
Package Description: | 1 BOTTLE in 1 CARTON (11822-0974-1) > 118 mL in 1 BOTTLE |
NDC Code | 11822-0974-1 |
Proprietary Name | childrens allergy relief |
Package Description | 1 BOTTLE in 1 CARTON (11822-0974-1) > 118 mL in 1 BOTTLE |
Product NDC | 11822-0974 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | cetirizine hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20080417 |
Marketing Category Name | ANDA |
Labeler Name | Rite Aid Corporation |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |