Product NDC: | 59779-106 |
Proprietary Name: | CVS |
Non Proprietary Name: | Cetirizine Hydrochloride |
Active Ingredient(s): | 5 mg/5mL & nbsp; Cetirizine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-106 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA201546 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110520 |
Package NDC: | 59779-106-08 |
Package Description: | 1 BOTTLE in 1 CARTON (59779-106-08) > 120 mL in 1 BOTTLE |
NDC Code | 59779-106-08 |
Proprietary Name | CVS |
Package Description | 1 BOTTLE in 1 CARTON (59779-106-08) > 120 mL in 1 BOTTLE |
Product NDC | 59779-106 |
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 | CVS Pharmacy |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |