Package 71335-0246-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0246-1
Digits Only 7133502461
Product NDC 71335-0246
Product ID 71335-0246_8a3da07e-0bfc-4d10-9dd9-11a19486fff7
Description

120 TABLET, FILM COATED in 1 BOTTLE (71335-0246-1)

Marketing

Marketing Status
Marketed Since 2017-10-04
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": "8a3da07e-0bfc-4d10-9dd9-11a19486fff7", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["93d117dd-e2bf-4daa-abe3-d4fefed3313c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0246-1)", "package_ndc": "71335-0246-1", "marketing_start_date": "20171004"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0246-2)", "package_ndc": "71335-0246-2", "marketing_start_date": "20171004"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0246-3)", "package_ndc": "71335-0246-3", "marketing_start_date": "20171004"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0246-4)", "package_ndc": "71335-0246-4", "marketing_start_date": "20171004"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0246-5)", "package_ndc": "71335-0246-5", "marketing_start_date": "20171004"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71335-0246_8a3da07e-0bfc-4d10-9dd9-11a19486fff7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-0246", "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": "ANDA088619", "marketing_category": "ANDA", "marketing_start_date": "20121022", "listing_expiration_date": "20261231"}