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Quality Choice - 63868-106-08 - (Cetirizine Hydrochloride)

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Drug Information of Quality Choice

Product NDC: 63868-106
Proprietary Name: Quality Choice
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 Quality Choice

Product NDC: 63868-106
Labeler Name: Chain Drug Marketing Association
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA201546
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Quality Choice

Package NDC: 63868-106-08
Package Description: 1 BOTTLE in 1 CARTON (63868-106-08) > 120 mL in 1 BOTTLE

NDC Information of Quality Choice

NDC Code 63868-106-08
Proprietary Name Quality Choice
Package Description 1 BOTTLE in 1 CARTON (63868-106-08) > 120 mL in 1 BOTTLE
Product NDC 63868-106
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 Chain Drug Marketing Association
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Quality Choice


General Information