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Cetirizine Hydrochloride - 0904-5852-61 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 0904-5852
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 0904-5852
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078317
Marketing Category: ANDA
Start Marketing Date: 20071227

Package Information of Cetirizine Hydrochloride

Package NDC: 0904-5852-61
Package Description: 100 TABLET, FILM COATED in 1 BLISTER PACK (0904-5852-61)

NDC Information of Cetirizine Hydrochloride

NDC Code 0904-5852-61
Proprietary Name Cetirizine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BLISTER PACK (0904-5852-61)
Product NDC 0904-5852
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20071227
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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