Package 42806-160-05

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-160-05
Digits Only 4280616005
Product NDC 42806-160
Description

500 TABLET, FILM COATED in 1 BOTTLE (42806-160-05)

Marketing

Marketing Status
Marketed Since 2015-03-31
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": "5e33c30d-cf33-4d61-98ca-eab9aab2ddf3", "openfda": {"upc": ["0342806160015"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["82b015dc-999c-46a4-bcaa-a4c81a193b68"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-160-01)", "package_ndc": "42806-160-01", "marketing_start_date": "20150331"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42806-160-05)", "package_ndc": "42806-160-05", "marketing_start_date": "20150331"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42806-160-10)", "package_ndc": "42806-160-10", "marketing_start_date": "20150331"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "42806-160_5e33c30d-cf33-4d61-98ca-eab9aab2ddf3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "42806-160", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}