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Cetirizine Hydrochloride - 52549-2106-1 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 52549-2106
Proprietary Name: 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)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 52549-2106
Labeler Name: Taro Pharmaceutical Industries, Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA201546
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Cetirizine Hydrochloride

Package NDC: 52549-2106-1
Package Description: 1 BOTTLE in 1 CARTON (52549-2106-1) > 237 mL in 1 BOTTLE

NDC Information of Cetirizine Hydrochloride

NDC Code 52549-2106-1
Proprietary Name Cetirizine Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (52549-2106-1) > 237 mL in 1 BOTTLE
Product NDC 52549-2106
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 Taro Pharmaceutical Industries, Ltd.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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