Package 50090-7330-6

{"route": ["ORAL"], "spl_id": "4278def4-d310-40ba-a058-2b4f21b9d8ec", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["69a58bc6-c8a4-48ad-ac77-90fac42e0398"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0)", "package_ndc": "50090-7330-0", "marketing_start_date": "20241015"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1)", "package_ndc": "50090-7330-1", "marketing_start_date": "20241015"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7330-4)", "package_ndc": "50090-7330-4", "marketing_start_date": "20241015"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-7330-6)", "package_ndc": "50090-7330-6", "marketing_start_date": "20241015"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "50090-7330_4278def4-d310-40ba-a058-2b4f21b9d8ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7330", "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"}