Package 70954-912-10

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70954-912-10
Digits Only 7095491210
Product NDC 70954-912
Product ID 70954-912_43889411-a303-41a1-b03b-1ee46f452c54
Description

473 mL in 1 BOTTLE (70954-912-10)

Marketing

Marketing Status
Marketed Since 2026-01-15
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": "43889411-a303-41a1-b03b-1ee46f452c54", "openfda": {"upc": ["0370954912101"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["43889411-a303-41a1-b03b-1ee46f452c54"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (70954-912-10)", "package_ndc": "70954-912-10", "marketing_start_date": "20260115"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "70954-912_43889411-a303-41a1-b03b-1ee46f452c54", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70954-912", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA219648", "marketing_category": "ANDA", "marketing_start_date": "20260115", "listing_expiration_date": "20261231"}