Package 51407-969-10

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-969-10
Digits Only 5140796910
Product NDC 51407-969
Description

1000 TABLET in 1 BOTTLE (51407-969-10)

Marketing

Marketing Status
Marketed Since 2025-03-04
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38f9f6f8-8eb8-450b-e063-6394a90a5f38", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["2fc9b08a-e675-dbc5-e063-6294a90ad054"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (51407-969-10)", "package_ndc": "51407-969-10", "marketing_start_date": "20250304"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "51407-969_38f9f6f8-8eb8-450b-e063-6394a90a5f38", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51407-969", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}