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Cetirizine Hydrochloride - 51079-597-20 - (cetirizine hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 51079-597
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: 51079-597
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076677
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Cetirizine Hydrochloride

Package NDC: 51079-597-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)

NDC Information of Cetirizine Hydrochloride

NDC Code 51079-597-20
Proprietary Name Cetirizine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)
Product NDC 51079-597
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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