Package 60505-0169-7

{"route": ["ORAL"], "spl_id": "4ee96b96-8019-3bb3-6737-f6f88c6289d9", "openfda": {"upc": ["0360505132393"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["dcf45e4f-b46e-6fbb-b67a-2ff619ab1780"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-0169-1)", "package_ndc": "60505-0169-1", "marketing_start_date": "20110718"}, {"sample": false, "description": "20000 TABLET in 1 BOTTLE (60505-0169-2)", "package_ndc": "60505-0169-2", "marketing_start_date": "20110718"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (60505-0169-5)", "package_ndc": "60505-0169-5", "marketing_start_date": "20110718"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (60505-0169-7)", "package_ndc": "60505-0169-7", "marketing_start_date": "20110718"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (60505-0169-9)", "package_ndc": "60505-0169-9", "marketing_start_date": "20110718"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "60505-0169_4ee96b96-8019-3bb3-6737-f6f88c6289d9", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "60505-0169", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20271231"}