Package 69452-395-88

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride oral
NDC Package

Package Facts

Identity

Package NDC 69452-395-88
Digits Only 6945239588
Product NDC 69452-395
Product ID 69452-395_39f93640-6535-6c3b-e063-6394a90a7f2d
Description

473 mL in 1 BOTTLE (69452-395-88)

Marketing

Marketing Status
Marketed Since 2025-07-17
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride oral
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": "39f93640-6535-6c3b-e063-6394a90a7f2d", "openfda": {"upc": ["0369452395882"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["39f93633-000e-6c3f-e063-6394a90a5a0b"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (69452-395-88)", "package_ndc": "69452-395-88", "marketing_start_date": "20250717"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "69452-395_39f93640-6535-6c3b-e063-6394a90a7f2d", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "69452-395", "generic_name": "Hydroxyzine Hydrochloride Oral", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA219289", "marketing_category": "ANDA", "marketing_start_date": "20250717", "listing_expiration_date": "20261231"}