Package 72189-542-90

{"route": ["ORAL"], "spl_id": "4615ec4d-f6e1-70c0-e063-6394a90a154f", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["13673a09-8a50-5cd0-e063-6294a90a3d5b"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-542-30)", "package_ndc": "72189-542-30", "marketing_start_date": "20240311"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-542-90)", "package_ndc": "72189-542-90", "marketing_start_date": "20240311"}], "brand_name": "Finasteride", "product_id": "72189-542_4615ec4d-f6e1-70c0-e063-6394a90a154f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "72189-542", "generic_name": "Finasteride", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA204304", "marketing_category": "ANDA", "marketing_start_date": "20240311", "listing_expiration_date": "20261231"}