Package 71335-2410-5

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2410-5
Digits Only 7133524105
Product NDC 71335-2410
Product ID 71335-2410_628ecb39-d59f-44d7-8d84-6dd5d31407c1
Description

90 TABLET, FILM COATED in 1 BOTTLE (71335-2410-5)

Marketing

Marketing Status
Marketed Since 2024-06-10
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": "628ecb39-d59f-44d7-8d84-6dd5d31407c1", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["4b8614d9-335c-4141-aaed-445c604ba08c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2410-1)", "package_ndc": "71335-2410-1", "marketing_start_date": "20240610"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2410-2)", "package_ndc": "71335-2410-2", "marketing_start_date": "20240610"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2410-3)", "package_ndc": "71335-2410-3", "marketing_start_date": "20240610"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2410-4)", "package_ndc": "71335-2410-4", "marketing_start_date": "20240610"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2410-5)", "package_ndc": "71335-2410-5", "marketing_start_date": "20240610"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "71335-2410_628ecb39-d59f-44d7-8d84-6dd5d31407c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-2410", "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": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}