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Cetirizine Hydrochloride - 55111-700-16 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 55111-700
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: 55111-700
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078870
Marketing Category: ANDA
Start Marketing Date: 20090820

Package Information of Cetirizine Hydrochloride

Package NDC: 55111-700-16
Package Description: 480 mL in 1 BOTTLE (55111-700-16)

NDC Information of Cetirizine Hydrochloride

NDC Code 55111-700-16
Proprietary Name Cetirizine Hydrochloride
Package Description 480 mL in 1 BOTTLE (55111-700-16)
Product NDC 55111-700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20090820
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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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