Package 55154-0194-0

Brand: cetirizine

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-0194-0
Digits Only 5515401940
Product NDC 55154-0194
Description

10 BLISTER PACK in 1 BAG (55154-0194-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-11-07
Brand cetirizine
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "702ba3a1-5769-4e93-b213-e79a5f408c1d", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["37c6d1e4-dd88-42a2-a828-539b68aa5dad"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-0194-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-0194-0", "marketing_start_date": "20251107"}], "brand_name": "Cetirizine", "product_id": "55154-0194_702ba3a1-5769-4e93-b213-e79a5f408c1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55154-0194", "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_start_date": "20251107", "listing_expiration_date": "20271231"}