Package 72189-333-72

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-333-72
Digits Only 7218933372
Product NDC 72189-333
Description

120 TABLET in 1 BOTTLE (72189-333-72)

Marketing

Marketing Status
Marketed Since 2022-03-03
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": "40817dfb-a4b8-2d36-e063-6394a90ac107", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["d956063a-ef48-faca-e053-2995a90a0291"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-333-30)", "package_ndc": "72189-333-30", "marketing_start_date": "20220303"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-333-72)", "package_ndc": "72189-333-72", "marketing_start_date": "20220303"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "72189-333_40817dfb-a4b8-2d36-e063-6394a90ac107", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72189-333", "generic_name": "HYDROXYZINE HYDROCHLORIDE", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20220303", "listing_expiration_date": "20261231"}