Package 55154-5399-0

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-5399-0
Digits Only 5515453990
Product NDC 55154-5399
Description

10 BLISTER PACK in 1 BAG (55154-5399-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

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": "897f5838-b1e4-472f-9348-f001dd1d5f22", "openfda": {"upc": ["0055154539906"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0b0190c7-acfd-4140-bcaf-9fe835ebaf49"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-5399-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-5399-0", "marketing_start_date": "20120330"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "55154-5399_897f5838-b1e4-472f-9348-f001dd1d5f22", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55154-5399", "generic_name": "cetirizine hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "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"}