Package 47335-714-81

{"route": ["ORAL"], "spl_id": "3fb7fc89-95b5-4c8a-9b1c-dd509cadb4eb", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["abd87058-923f-4767-986c-278201c0e688"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)", "package_ndc": "47335-714-08", "marketing_start_date": "20221123"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)", "package_ndc": "47335-714-18", "marketing_start_date": "20221123"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)", "package_ndc": "47335-714-81", "marketing_start_date": "20221123"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)", "package_ndc": "47335-714-83", "marketing_start_date": "20221123"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)", "package_ndc": "47335-714-88", "marketing_start_date": "20221123"}], "brand_name": "Finasteride", "product_id": "47335-714_3fb7fc89-95b5-4c8a-9b1c-dd509cadb4eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "47335-714", "generic_name": "Finasteride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA090508", "marketing_category": "ANDA", "marketing_start_date": "20221123", "listing_expiration_date": "20261231"}