Package 72789-378-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-378-30
Digits Only 7278937830
Product NDC 72789-378
Product ID 72789-378_3807de87-ff3b-f62b-e063-6294a90aca9f
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-378-30)

Marketing

Marketing Status
Marketed Since 2024-02-02
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": "3807de87-ff3b-f62b-e063-6294a90aca9f", "openfda": {"upc": ["0372789378305"], "unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["44c63e67-a9e0-4a4f-b34e-2ca60a981766"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-378-30)", "package_ndc": "72789-378-30", "marketing_start_date": "20240202"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "72789-378_3807de87-ff3b-f62b-e063-6294a90aca9f", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72789-378", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}