Package 72162-2513-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2513-0
Digits Only 7216225130
Product NDC 72162-2513
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72162-2513-0)

Marketing

Marketing Status
Marketed Since 2025-05-23
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c8cab0b8-d63c-4e62-b95e-c174b0b663c9", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["a8c83479-f919-49f9-b125-747bd0e3211c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2513-0)", "package_ndc": "72162-2513-0", "marketing_start_date": "20250523"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2513-1)", "package_ndc": "72162-2513-1", "marketing_start_date": "20250523"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2513-5)", "package_ndc": "72162-2513-5", "marketing_start_date": "20250523"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72162-2513_c8cab0b8-d63c-4e62-b95e-c174b0b663c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72162-2513", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20211007", "listing_expiration_date": "20261231"}