Package 70518-2807-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2807-0
Digits Only 7051828070
Product NDC 70518-2807
Product ID 70518-2807_4aa35fdf-9b24-64c4-e063-6294a90a7e60
Description

30 TABLET in 1 BLISTER PACK (70518-2807-0)

Marketing

Marketing Status
Marketed Since 2020-07-08
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4aa35fdf-9b24-64c4-e063-6294a90a7e60", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["71eea118-395c-4559-aed5-900b635674b8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2807-0)", "package_ndc": "70518-2807-0", "marketing_start_date": "20200708"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "70518-2807_4aa35fdf-9b24-64c4-e063-6294a90a7e60", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-2807", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20200708", "listing_expiration_date": "20271231"}