Package 70518-4360-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4360-0
Digits Only 7051843600
Product NDC 70518-4360
Description

30 TABLET in 1 BLISTER PACK (70518-4360-0)

Marketing

Marketing Status
Marketed Since 2025-06-16
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": "37c4a121-e66d-5ef1-e063-6294a90a15cc", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["58d99cf6-2319-410b-b8be-de9c304541b6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4360-0)", "package_ndc": "70518-4360-0", "marketing_start_date": "20250616"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "70518-4360_37c4a121-e66d-5ef1-e063-6294a90a15cc", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-4360", "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": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20250616", "listing_expiration_date": "20261231"}