Package 50090-6655-4

{"route": ["ORAL"], "spl_id": "55f40911-dfa2-4c85-8faa-a0d9ec530be1", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["3d5d3ebf-e57e-4ed1-be97-d4b299fb738d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-6655-0)", "package_ndc": "50090-6655-0", "marketing_start_date": "20230830"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6655-1)", "package_ndc": "50090-6655-1", "marketing_start_date": "20230830"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6655-4)", "package_ndc": "50090-6655-4", "marketing_start_date": "20230830"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-6655-6)", "package_ndc": "50090-6655-6", "marketing_start_date": "20230830"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "50090-6655_55f40911-dfa2-4c85-8faa-a0d9ec530be1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-6655", "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"}