Package 65162-062-05

{"route": ["ORAL"], "spl_id": "71ed86a3-ff8a-4545-9bae-26632466fd80", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["4350b771-76a9-4e00-93f0-a18c71288f83"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (65162-062-05)", "package_ndc": "65162-062-05", "marketing_start_date": "20191202"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 TRAY (65162-062-48)  / 10 mL in 1 CUP, UNIT-DOSE (65162-062-47)", "package_ndc": "65162-062-48", "marketing_start_date": "20191202"}], "brand_name": "Sucralfate", "product_id": "65162-062_71ed86a3-ff8a-4545-9bae-26632466fd80", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "65162-062", "generic_name": "Sucralfate Oral", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA209356", "marketing_category": "ANDA", "marketing_start_date": "20191202", "listing_expiration_date": "20261231"}