Package 68788-8872-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8872-3
Digits Only 6878888723
Product NDC 68788-8872
Product ID 68788-8872_a35d1fe2-328d-42ff-ba1f-18a7f2f03c88
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)

Marketing

Marketing Status
Marketed Since 2025-05-01
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": "a35d1fe2-328d-42ff-ba1f-18a7f2f03c88", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["a35d1fe2-328d-42ff-ba1f-18a7f2f03c88"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)", "package_ndc": "68788-8872-3", "marketing_start_date": "20250501"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "68788-8872_a35d1fe2-328d-42ff-ba1f-18a7f2f03c88", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68788-8872", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}