Package 57664-441-88

{"route": ["ORAL"], "spl_id": "47e1a46c-562d-ac4c-e063-6294a90a9b81", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604", "197606"], "spl_set_id": ["62795623-a2bc-4dd2-8989-3b9782bfd80e"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (57664-441-18)", "package_ndc": "57664-441-18", "marketing_start_date": "20150217"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-441-88)", "package_ndc": "57664-441-88", "marketing_start_date": "20150217"}], "brand_name": "Digoxin", "product_id": "57664-441_47e1a46c-562d-ac4c-e063-6294a90a9b81", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "57664-441", "generic_name": "Digoxin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "250 ug/1"}], "application_number": "ANDA076363", "marketing_category": "ANDA", "marketing_start_date": "20150217", "listing_expiration_date": "20271231"}