Package 80425-0173-1
Brand: hydroxyzine hcl
Generic: hydroxyzine hclPackage Facts
Identity
Package NDC
80425-0173-1
Digits Only
8042501731
Product NDC
80425-0173
Description
30 TABLET, FILM COATED in 1 BOTTLE (80425-0173-1)
Marketing
Marketing Status
Brand
hydroxyzine hcl
Generic
hydroxyzine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16edd342-ced2-eeb7-e063-6394a90a35ef", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["cd4ea0ea-0d92-b70c-e053-2995a90a62ce"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0173-1)", "package_ndc": "80425-0173-1", "marketing_start_date": "20130219"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0173-2)", "package_ndc": "80425-0173-2", "marketing_start_date": "20240425"}], "brand_name": "Hydroxyzine HCL", "product_id": "80425-0173_16edd342-ced2-eeb7-e063-6394a90a35ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "80425-0173", "generic_name": "Hydroxyzine HCL", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine HCL", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA088619", "marketing_category": "ANDA", "marketing_start_date": "20121022", "listing_expiration_date": "20261231"}