Package 55154-8081-0

Brand: cetirizine

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-8081-0
Digits Only 5515480810
Product NDC 55154-8081
Description

10 BLISTER PACK in 1 BAG (55154-8081-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-06-30
Brand cetirizine
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01be285f-cde9-4c0f-ba29-ca2f40db78f0", "openfda": {"upc": ["0055154808101"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["6f3c2e57-7a0f-432f-a7f1-04906f5e4ddf"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-8081-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-8081-0", "marketing_end_date": "20260630", "marketing_start_date": "20180629"}], "brand_name": "Cetirizine", "product_id": "55154-8081_01be285f-cde9-4c0f-ba29-ca2f40db78f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55154-8081", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20180629"}