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Cetirizine Hydrochloride - 27808-001-02 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 27808-001
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 27808-001
Labeler Name: Tris Pharma Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090572
Marketing Category: ANDA
Start Marketing Date: 20121121

Package Information of Cetirizine Hydrochloride

Package NDC: 27808-001-02
Package Description: 118 mL in 1 BOTTLE, GLASS (27808-001-02)

NDC Information of Cetirizine Hydrochloride

NDC Code 27808-001-02
Proprietary Name Cetirizine Hydrochloride
Package Description 118 mL in 1 BOTTLE, GLASS (27808-001-02)
Product NDC 27808-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121121
Marketing Category Name ANDA
Labeler Name Tris Pharma Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


General Information