Package 60219-1656-5

{"route": ["ORAL"], "spl_id": "3595f982-2982-4ab0-838a-4cada5e1337b", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0360219165618"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["b2e07ac7-4a8a-4b68-bb65-167d1aa86883"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60219-1656-1)", "package_ndc": "60219-1656-1", "marketing_start_date": "20240302"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (60219-1656-5)", "package_ndc": "60219-1656-5", "marketing_start_date": "20240302"}], "brand_name": "Sucralfate", "product_id": "60219-1656_3595f982-2982-4ab0-838a-4cada5e1337b", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "60219-1656", "generic_name": "Sucralfate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215576", "marketing_category": "ANDA", "marketing_start_date": "20240302", "listing_expiration_date": "20261231"}