Package 0904-6707-82

{"route": ["ORAL"], "spl_id": "861910dd-653c-4652-b0e8-e78fa95ab8d9", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["42fefb90-6941-4539-8f32-df1896223450"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6707-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6707-06", "marketing_end_date": "20261231", "marketing_start_date": "20170929"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6707-82)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6707-82", "marketing_end_date": "20261231", "marketing_start_date": "20170929"}], "brand_name": "Sevelamer Carbonate", "product_id": "0904-6707_861910dd-653c-4652-b0e8-e78fa95ab8d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0904-6707", "generic_name": "Sevelamer Carbonate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA206094", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20170929"}