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Cetirizine Hydrochloride - 54838-552-40 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 54838-552
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): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 54838-552
Labeler Name: Silarx Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091130
Marketing Category: ANDA
Start Marketing Date: 20110502

Package Information of Cetirizine Hydrochloride

Package NDC: 54838-552-40
Package Description: 120 mL in 1 CARTON (54838-552-40)

NDC Information of Cetirizine Hydrochloride

NDC Code 54838-552-40
Proprietary Name Cetirizine Hydrochloride
Package Description 120 mL in 1 CARTON (54838-552-40)
Product NDC 54838-552
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110502
Marketing Category Name ANDA
Labeler Name Silarx Pharmaceuticals, Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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