Package 81033-149-44

{"route": ["ORAL"], "spl_id": "36d940f2-207c-68c5-e063-6294a90a6b4a", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["36d940f2-207b-68c5-e063-6294a90a6b4a"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44)  / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)", "package_ndc": "81033-149-44", "marketing_start_date": "20240701"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-149-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)", "package_ndc": "81033-149-52", "marketing_start_date": "20240701"}], "brand_name": "Sucralfate", "product_id": "81033-149_36d940f2-207c-68c5-e063-6294a90a6b4a", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "81033-149", "generic_name": "Sucralfate", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216474", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}