Package 50090-7329-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7329-0
Digits Only 5009073290
Product NDC 50090-7329
Product ID 50090-7329_344bc91e-a875-4a60-96ff-cdd4816d7c11
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7329-0)

Marketing

Marketing Status
Marketed Since 2024-10-15
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "344bc91e-a875-4a60-96ff-cdd4816d7c11", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["afa74394-c079-4ad3-b555-270fe0de3d62"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7329-0)", "package_ndc": "50090-7329-0", "marketing_start_date": "20241015"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "50090-7329_344bc91e-a875-4a60-96ff-cdd4816d7c11", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7329", "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": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}