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cetirizine hydrochloride - 57664-181-34 - (cetirizine hydrochloride)

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Drug Information of cetirizine hydrochloride

Product NDC: 57664-181
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): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of cetirizine hydrochloride

Product NDC: 57664-181
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090191
Marketing Category: ANDA
Start Marketing Date: 20091116

Package Information of cetirizine hydrochloride

Package NDC: 57664-181-34
Package Description: 473 mL in 1 BOTTLE, GLASS (57664-181-34)

NDC Information of cetirizine hydrochloride

NDC Code 57664-181-34
Proprietary Name cetirizine hydrochloride
Package Description 473 mL in 1 BOTTLE, GLASS (57664-181-34)
Product NDC 57664-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20091116
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of cetirizine hydrochloride


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