Package 50090-6657-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6657-0
Digits Only 5009066570
Product NDC 50090-6657
Product ID 50090-6657_f8934174-e679-418a-a77c-9d3c57f15ce4
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6657-0)

Marketing

Marketing Status
Marketed Since 2023-08-30
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": "f8934174-e679-418a-a77c-9d3c57f15ce4", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["e83de74d-b2e0-45c5-b072-170a96216d3a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6657-0)", "package_ndc": "50090-6657-0", "marketing_start_date": "20230830"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "50090-6657_f8934174-e679-418a-a77c-9d3c57f15ce4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-6657", "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": "ANDA040602", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}