Package 0904-6617-61

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6617-61
Digits Only 0904661761
Product NDC 0904-6617
Product ID 0904-6617_f78ac709-6b0b-438b-8333-bd4a7509cfed
Description

100 BLISTER PACK in 1 CARTON (0904-6617-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-08-31
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": "f78ac709-6b0b-438b-8333-bd4a7509cfed", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258", "995281"], "spl_set_id": ["7534a3bb-b4cd-415f-8612-53b37dc6d55f"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6617-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6617-61", "marketing_end_date": "20260831", "marketing_start_date": "20150331"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "0904-6617_f78ac709-6b0b-438b-8333-bd4a7509cfed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0904-6617", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20150331"}