Package 0904-7377-40

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7377-40
Digits Only 0904737740
Product NDC 0904-7377
Product ID 0904-7377_462940f7-5dba-4ca2-829d-e0a8a72579e5
Description

500 TABLET in 1 BOTTLE (0904-7377-40)

Marketing

Marketing Status
Discontinued 2026-04-30
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": "462940f7-5dba-4ca2-829d-e0a8a72579e5", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["7f76580c-96a0-4b56-8986-ff5488bb9869"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (0904-7377-40)", "package_ndc": "0904-7377-40", "marketing_end_date": "20260430", "marketing_start_date": "20230801"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "0904-7377_462940f7-5dba-4ca2-829d-e0a8a72579e5", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0904-7377", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Major Pharmaceuticals", "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_end_date": "20260430", "marketing_start_date": "20230801"}