Package 50090-6659-0

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6659-0
Digits Only 5009066590
Product NDC 50090-6659
Product ID 50090-6659_ef93bd62-a353-485a-aeff-7868363aad86
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6659-0)

Marketing

Marketing Status
Marketed Since 2023-08-30
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": "ef93bd62-a353-485a-aeff-7868363aad86", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["49ee4ecf-b2c0-4301-89da-111e4d853168"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6659-0)", "package_ndc": "50090-6659-0", "marketing_start_date": "20230830"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "50090-6659_ef93bd62-a353-485a-aeff-7868363aad86", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-6659", "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"}