Package 72189-577-60

Brand: hydroxyzine hcl

Generic: hydroxyzine hcl
NDC Package

Package Facts

Identity

Package NDC 72189-577-60
Digits Only 7218957760
Product NDC 72189-577
Product ID 72189-577_22049012-733f-6b45-e063-6294a90a670f
Description

60 TABLET, FILM COATED in 1 BOTTLE (72189-577-60)

Marketing

Marketing Status
Marketed Since 2024-09-13
Brand hydroxyzine hcl
Generic hydroxyzine hcl
Sample Package No

Linked Drug Pages (1)

Hydroxyzine HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "22049012-733f-6b45-e063-6294a90a670f", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["22049012-733e-6b45-e063-6294a90a670f"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-577-60)", "package_ndc": "72189-577-60", "marketing_start_date": "20240913"}], "brand_name": "Hydroxyzine HCL", "product_id": "72189-577_22049012-733f-6b45-e063-6294a90a670f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72189-577", "generic_name": "Hydroxyzine HCL", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine HCL", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20240913", "listing_expiration_date": "20261231"}