Package 54838-502-80

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54838-502-80
Digits Only 5483850280
Product NDC 54838-502
Description

473 mL in 1 BOTTLE, PLASTIC (54838-502-80)

Marketing

Marketing Status
Marketed Since 2013-08-21
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": "823645dc-4e60-4279-97fa-ca0d1c1d7ad8", "openfda": {"upc": ["0354838502800"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["a4fb61ae-aad6-4bd6-83fc-8b227f175df9"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (54838-502-80)", "package_ndc": "54838-502-80", "marketing_start_date": "20130821"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "54838-502_823645dc-4e60-4279-97fa-ca0d1c1d7ad8", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "54838-502", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201674", "marketing_category": "ANDA", "marketing_start_date": "20130821", "listing_expiration_date": "20261231"}