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Cetirizine Hydrochloride - 0378-3635-01 - (cetirizine hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 0378-3635
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: cetirizine hydrochloride
Active Ingredient(s): 5    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: 0378-3635
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076677
Marketing Category: ANDA
Start Marketing Date: 20091214

Package Information of Cetirizine Hydrochloride

Package NDC: 0378-3635-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3635-01)

NDC Information of Cetirizine Hydrochloride

NDC Code 0378-3635-01
Proprietary Name Cetirizine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3635-01)
Product NDC 0378-3635
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091214
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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