HealthMart - 62011-0180-1 - (Cetirizine Hydrochloride)

Alphabetical Index


Drug Information of HealthMart

Product NDC: 62011-0180
Proprietary Name: HealthMart
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)

Labeler Information of HealthMart

Product NDC: 62011-0180
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090182
Marketing Category: ANDA
Start Marketing Date: 20110908

Package Information of HealthMart

Package NDC: 62011-0180-1
Package Description: 1 BOTTLE in 1 CARTON (62011-0180-1) > 120 mL in 1 BOTTLE

NDC Information of HealthMart

NDC Code 62011-0180-1
Proprietary Name HealthMart
Package Description 1 BOTTLE in 1 CARTON (62011-0180-1) > 120 mL in 1 BOTTLE
Product NDC 62011-0180
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110908
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of HealthMart


General Information