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cetirizine hydrochloride - 29300-134-19 - (cetirizine hydrochloride)

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Drug Information of cetirizine hydrochloride

Product NDC: 29300-134
Proprietary Name: cetirizine hydrochloride
Non Proprietary Name: cetirizine hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   cetirizine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of cetirizine hydrochloride

Product NDC: 29300-134
Labeler Name: Unichem Pharmaceuticals (USA), Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078680
Marketing Category: ANDA
Start Marketing Date: 20101130

Package Information of cetirizine hydrochloride

Package NDC: 29300-134-19
Package Description: 1 BOTTLE in 1 CARTON (29300-134-19) > 90 TABLET in 1 BOTTLE

NDC Information of cetirizine hydrochloride

NDC Code 29300-134-19
Proprietary Name cetirizine hydrochloride
Package Description 1 BOTTLE in 1 CARTON (29300-134-19) > 90 TABLET in 1 BOTTLE
Product NDC 29300-134
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101130
Marketing Category Name ANDA
Labeler Name Unichem Pharmaceuticals (USA), Inc.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of cetirizine hydrochloride


General Information