Package 50090-7331-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7331-0
Digits Only 5009073310
Product NDC 50090-7331
Product ID 50090-7331_fe69a194-e17b-4a41-b273-85e126eb7619
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7331-0)

Marketing

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

Linked Drug Pages (1)

HYDROXYZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fe69a194-e17b-4a41-b273-85e126eb7619", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["a9a133e6-efce-4bdb-9335-49c74e57fafe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7331-0)", "package_ndc": "50090-7331-0", "marketing_start_date": "20241015"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "50090-7331_fe69a194-e17b-4a41-b273-85e126eb7619", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7331", "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"}