Package 50090-3583-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3583-1
Digits Only 5009035831
Product NDC 50090-3583
Description

28 TABLET in 1 BOTTLE (50090-3583-1)

Marketing

Marketing Status
Marketed Since 2018-09-21
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": "7606c767-4ce5-4ea2-b51c-d9c483e916fa", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["80e60583-76d3-4e65-8581-4cdaff7cd1c1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-3583-1)", "package_ndc": "50090-3583-1", "marketing_start_date": "20180921"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "50090-3583_7606c767-4ce5-4ea2-b51c-d9c483e916fa", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-3583", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}