Package 23155-501-10

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 23155-501-10
Digits Only 2315550110
Product NDC 23155-501
Description

1000 TABLET in 1 BOTTLE (23155-501-10)

Marketing

Marketing Status
Marketed Since 2014-08-20
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be52341-592e-4a89-acc0-730b0560b132", "openfda": {"upc": ["0323155500011", "0323155502015", "0323155501018"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["f9ff4b7c-dc81-47af-8371-5c681eb0d876"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-501-01)", "package_ndc": "23155-501-01", "marketing_start_date": "20140820"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-501-05)", "package_ndc": "23155-501-05", "marketing_start_date": "20140820"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-501-10)", "package_ndc": "23155-501-10", "marketing_start_date": "20140820"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "23155-501_2be52341-592e-4a89-acc0-730b0560b132", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "23155-501", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}