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Cetirizine Hydrochloride HIVES - 57664-246-34 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride HIVES

Product NDC: 57664-246
Proprietary Name: Cetirizine Hydrochloride HIVES
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride HIVES

Product NDC: 57664-246
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091327
Marketing Category: ANDA
Start Marketing Date: 20111201

Package Information of Cetirizine Hydrochloride HIVES

Package NDC: 57664-246-34
Package Description: 470 mL in 1 BOTTLE (57664-246-34)

NDC Information of Cetirizine Hydrochloride HIVES

NDC Code 57664-246-34
Proprietary Name Cetirizine Hydrochloride HIVES
Package Description 470 mL in 1 BOTTLE (57664-246-34)
Product NDC 57664-246
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20111201
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride HIVES


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