Package 0615-8564-39

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8564-39
Digits Only 0615856439
Product NDC 0615-8564
Product ID 0615-8564_1ab953e6-830e-4845-8cca-9864f8002cdf
Description

30 TABLET in 1 BLISTER PACK (0615-8564-39)

Marketing

Marketing Status
Marketed Since 2025-02-06
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": "1ab953e6-830e-4845-8cca-9864f8002cdf", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["0c687cbe-ce40-4bc0-b880-5166b5be7a80"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8564-39)", "package_ndc": "0615-8564-39", "marketing_start_date": "20250206"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "0615-8564_1ab953e6-830e-4845-8cca-9864f8002cdf", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0615-8564", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "20140820", "listing_expiration_date": "20261231"}