Package 80425-0394-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0394-1
Digits Only 8042503941
Product NDC 80425-0394
Product ID 80425-0394_19b094e5-8afa-94c1-e063-6294a90a297f
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0394-1)

Marketing

Marketing Status
Marketed Since 2024-05-24
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": "19b094e5-8afa-94c1-e063-6294a90a297f", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["19b08f92-da63-021f-e063-6394a90a16e2"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0394-1)", "package_ndc": "80425-0394-1", "marketing_start_date": "20240524"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0394-2)", "package_ndc": "80425-0394-2", "marketing_start_date": "20240524"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "80425-0394_19b094e5-8afa-94c1-e063-6294a90a297f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "80425-0394", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20240524", "listing_expiration_date": "20261231"}