Package 62135-575-05

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-575-05
Digits Only 6213557505
Product NDC 62135-575
Description

500 TABLET in 1 BOTTLE (62135-575-05)

Marketing

Marketing Status
Marketed Since 2023-04-11
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": "459c9507-ea13-81b1-e063-6394a90a3db4", "openfda": {"upc": ["0362135575052", "0362135574055", "0362135573126", "0362135573058", "0362135575120", "0362135574123"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["6533bb4f-efbc-4fca-b625-daa1b3978740"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (62135-575-05)", "package_ndc": "62135-575-05", "marketing_start_date": "20230411"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (62135-575-12)", "package_ndc": "62135-575-12", "marketing_start_date": "20230411"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "62135-575_459c9507-ea13-81b1-e063-6394a90a3db4", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-575", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "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"}