Package 59762-0170-6

{"route": ["ORAL"], "spl_id": "fdede630-529a-48fe-b796-59c3504c8d32", "openfda": {"upc": ["0359762017062", "0359762080028"], "unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["9e432622-2e6f-4cf8-892f-510288dd50f2"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59762-0170-1)", "package_ndc": "59762-0170-1", "marketing_end_date": "20260331", "marketing_start_date": "20140121"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59762-0170-6)", "package_ndc": "59762-0170-6", "marketing_end_date": "20260831", "marketing_start_date": "20140121"}], "brand_name": "Tolterodine Tartrate", "product_id": "59762-0170_fdede630-529a-48fe-b796-59c3504c8d32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "59762-0170", "generic_name": "Tolterodine Tartrate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "1 mg/1"}], "application_number": "NDA020771", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260831", "marketing_start_date": "20140121"}