Package 0093-0018-06

{"route": ["ORAL"], "spl_id": "2f429822-d6d2-43c0-9aaf-1270b3e92a2f", "openfda": {"unii": ["5T619TQR3R"], "rxcui": ["855178", "855194"], "spl_set_id": ["d27e25b5-5d02-419f-b098-41fb162c5872"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-0018-05)", "package_ndc": "0093-0018-05", "marketing_start_date": "20151101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0093-0018-06)", "package_ndc": "0093-0018-06", "marketing_start_date": "20151101"}], "brand_name": "Tolterodine Tartrate", "product_id": "0093-0018_2f429822-d6d2-43c0-9aaf-1270b3e92a2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0093-0018", "generic_name": "Tolterodine Tartrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolterodine Tartrate", "active_ingredients": [{"name": "TOLTERODINE TARTRATE", "strength": "2 mg/1"}], "application_number": "ANDA077006", "marketing_category": "ANDA", "marketing_start_date": "20151101", "listing_expiration_date": "20261231"}