Package 70518-2066-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2066-0
Digits Only 7051820660
Product NDC 70518-2066
Product ID 70518-2066_499c7349-9995-6589-e063-6394a90a0e58
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)

Marketing

Marketing Status
Marketed Since 2019-05-07
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": "499c7349-9995-6589-e063-6394a90a0e58", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["6ad55cd1-a284-4c3d-aa90-653704afdb75"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)", "package_ndc": "70518-2066-0", "marketing_start_date": "20190507"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "70518-2066_499c7349-9995-6589-e063-6394a90a0e58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-2066", "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": "ANDA088618", "marketing_category": "ANDA", "marketing_start_date": "20190507", "listing_expiration_date": "20271231"}