Package 70518-1692-2

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1692-2
Digits Only 7051816922
Product NDC 70518-1692
Product ID 70518-1692_496167aa-84ed-70f9-e063-6394a90ac9fb
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-1692-2)

Marketing

Marketing Status
Marketed Since 2024-09-13
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": "496167aa-84ed-70f9-e063-6394a90ac9fb", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["b6189074-e199-4f58-a78d-c04f131c13d9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-1692-2)", "package_ndc": "70518-1692-2", "marketing_start_date": "20240913"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "70518-1692_496167aa-84ed-70f9-e063-6394a90ac9fb", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-1692", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20181126", "listing_expiration_date": "20271231"}