Package 50090-7034-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7034-0
Digits Only 5009070340
Product NDC 50090-7034
Product ID 50090-7034_8a418e3b-7933-4ce1-af23-34277e341353
Description

100 BLISTER PACK in 1 CARTON (50090-7034-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-01-08
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8a418e3b-7933-4ce1-af23-34277e341353", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["c2bce6a4-9feb-4816-a6d8-151e8ef3314d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (50090-7034-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50090-7034-0", "marketing_start_date": "20240108"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "50090-7034_8a418e3b-7933-4ce1-af23-34277e341353", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7034", "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"}