Package 72162-2511-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2511-1
Digits Only 7216225111
Product NDC 72162-2511
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2511-1)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dfe85efe-65a5-4097-99cc-39db13e612a8", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["7c959515-a5a9-4d5e-90e9-bd58bc947330"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2511-1)", "package_ndc": "72162-2511-1", "marketing_start_date": "20250523"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2511-5)", "package_ndc": "72162-2511-5", "marketing_start_date": "20250523"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72162-2511_dfe85efe-65a5-4097-99cc-39db13e612a8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72162-2511", "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": "10 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20211007", "listing_expiration_date": "20261231"}