Package 51079-597-20

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-597-20
Digits Only 5107959720
Product NDC 51079-597
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)

Marketing

Marketing Status
Marketed Since 2012-03-30
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a39c300-d753-6884-e063-6394a90aa53e", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["bd0dc7f6-5fb9-4381-bd81-b150b75a2c68"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)", "package_ndc": "51079-597-20", "marketing_start_date": "20120330"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "51079-597_3a39c300-d753-6884-e063-6394a90aa53e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51079-597", "generic_name": "cetirizine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076677", "marketing_category": "ANDA", "marketing_start_date": "20120330", "listing_expiration_date": "20261231"}