Package 72162-2512-5

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2512-5
Digits Only 7216225125
Product NDC 72162-2512
Product ID 72162-2512_3dec3fc6-a125-4b46-86f9-7c42b2fe60ce
Description

500 TABLET, FILM COATED in 1 BOTTLE (72162-2512-5)

Marketing

Marketing Status
Marketed Since 2025-05-23
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": "3dec3fc6-a125-4b46-86f9-7c42b2fe60ce", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["e4e6a91d-f10b-4d85-a526-4c6192ea85dc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2512-0)", "package_ndc": "72162-2512-0", "marketing_start_date": "20250523"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2512-1)", "package_ndc": "72162-2512-1", "marketing_start_date": "20250523"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2512-5)", "package_ndc": "72162-2512-5", "marketing_start_date": "20250523"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72162-2512_3dec3fc6-a125-4b46-86f9-7c42b2fe60ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72162-2512", "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": "25 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20211007", "listing_expiration_date": "20261231"}