Package 55154-2148-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-2148-0
Digits Only 5515421480
Product NDC 55154-2148
Product ID 55154-2148_b4d274ce-d616-4835-80ce-76270524ed36
Description

10 BLISTER PACK in 1 BAG (55154-2148-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydroxyzine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4d274ce-d616-4835-80ce-76270524ed36", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["b4d274ce-d616-4835-80ce-76270524ed36"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2148-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-2148-0", "marketing_start_date": "20251022"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "55154-2148_b4d274ce-d616-4835-80ce-76270524ed36", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "55154-2148", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA088618", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}