Package 50090-7582-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7582-1
Digits Only 5009075821
Product NDC 50090-7582
Product ID 50090-7582_d0abf9e3-d92e-445f-b626-a81b499d6e47
Description

28 TABLET in 1 BOTTLE (50090-7582-1)

Marketing

Marketing Status
Marketed Since 2025-06-18
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": "d0abf9e3-d92e-445f-b626-a81b499d6e47", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["723b810b-46cc-4c45-ae1f-93ca358e007d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-7582-1)", "package_ndc": "50090-7582-1", "marketing_start_date": "20250618"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "50090-7582_d0abf9e3-d92e-445f-b626-a81b499d6e47", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7582", "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": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20091111", "listing_expiration_date": "20261231"}