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Cetirizine Hydrochloride - 55111-699-74 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 55111-699
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: 55111-699
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078343
Marketing Category: ANDA
Start Marketing Date: 20080115

Package Information of Cetirizine Hydrochloride

Package NDC: 55111-699-74
Package Description: 2 BLISTER PACK in 1 CARTON (55111-699-74) > 7 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Cetirizine Hydrochloride

NDC Code 55111-699-74
Proprietary Name Cetirizine Hydrochloride
Package Description 2 BLISTER PACK in 1 CARTON (55111-699-74) > 7 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55111-699
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080115
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


General Information