Package 50090-4117-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4117-0
Digits Only 5009041170
Product NDC 50090-4117
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-4117-0)

Marketing

Marketing Status
Marketed Since 2019-02-01
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1018a246-77e1-446e-b436-30feac311856", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["3946db7c-dc2d-4329-b9ac-f003d8c6d3e1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4117-0)", "package_ndc": "50090-4117-0", "marketing_start_date": "20190201"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4117-3)", "package_ndc": "50090-4117-3", "marketing_start_date": "20141128"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "50090-4117_1018a246-77e1-446e-b436-30feac311856", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-4117", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088617", "marketing_category": "ANDA", "marketing_start_date": "20130219", "listing_expiration_date": "20261231"}