Package 10135-718-12

{"route": ["ORAL"], "spl_id": "3e74abef-2742-2bbe-e063-6394a90a12cd", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904431"], "spl_set_id": ["b63421af-ec03-1de7-e053-2a95a90abec6"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (10135-718-12)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "10135-718-12", "marketing_start_date": "20201201"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (10135-718-44)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "10135-718-44", "marketing_start_date": "20201201"}], "brand_name": "Alendronate", "product_id": "10135-718_3e74abef-2742-2bbe-e063-6394a90a12cd", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "10135-718", "generic_name": "Alendronate sodium tablet", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090258", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}