Package 72162-2167-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2167-0
Digits Only 7216221670
Product NDC 72162-2167
Product ID 72162-2167_2a142721-6ffa-4c35-97f9-f563feb83a40
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72162-2167-0)

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "2a142721-6ffa-4c35-97f9-f563feb83a40", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["5ff091be-6e30-4305-a172-769ee45e110b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2167-0)", "package_ndc": "72162-2167-0", "marketing_start_date": "20231207"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72162-2167_2a142721-6ffa-4c35-97f9-f563feb83a40", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72162-2167", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}