Package 70518-0425-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-0425-1
Digits Only 7051804251
Product NDC 70518-0425
Product ID 70518-0425_47f6232c-ffab-56fb-e063-6394a90a1998
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-0425-1)

Marketing

Marketing Status
Marketed Since 2021-11-17
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": "47f6232c-ffab-56fb-e063-6394a90a1998", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["2dcc6b0c-b63c-4dc1-a517-bb60ff557c00"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0425-1)", "package_ndc": "70518-0425-1", "marketing_start_date": "20211117"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "70518-0425_47f6232c-ffab-56fb-e063-6394a90a1998", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-0425", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20170414", "listing_expiration_date": "20271231"}