Package 72162-1332-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1332-3
Digits Only 7216213323
Product NDC 72162-1332
Product ID 72162-1332_7adc75c5-71d2-48c2-9137-62e4533c7aed
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-1332-3)

Marketing

Marketing Status
Marketed Since 2024-04-08
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": "7adc75c5-71d2-48c2-9137-62e4533c7aed", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["dd9e5dc5-720c-4de8-abae-6404c31f341f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1332-3)", "package_ndc": "72162-1332-3", "marketing_start_date": "20240408"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-1332-9)", "package_ndc": "72162-1332-9", "marketing_start_date": "20240408"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72162-1332_7adc75c5-71d2-48c2-9137-62e4533c7aed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72162-1332", "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": "ANDA040600", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}