Package 80425-0376-2

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0376-2
Digits Only 8042503762
Product NDC 80425-0376
Product ID 80425-0376_18aaed76-71d1-24f8-e063-6394a90aae0f
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0376-2)

Marketing

Marketing Status
Marketed Since 2024-04-25
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": "18aaed76-71d1-24f8-e063-6394a90aae0f", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["138ec5c1-bb06-2a82-e063-6394a90ab42b"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0376-1)", "package_ndc": "80425-0376-1", "marketing_start_date": "20240313"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0376-2)", "package_ndc": "80425-0376-2", "marketing_start_date": "20240425"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "80425-0376_18aaed76-71d1-24f8-e063-6394a90aae0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "80425-0376", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20240313", "listing_expiration_date": "20261231"}