Package 81033-017-51

{"route": ["ORAL"], "spl_id": "334a40cd-5521-39e3-e063-6394a90ab024", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["XF417D3PSL", "1Q73Q2JULR"], "rxcui": ["543014"], "spl_set_id": ["3140f8fe-0644-7561-e063-6394a90a2c28"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-017-50)  / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15)", "package_ndc": "81033-017-50", "marketing_start_date": "20250401"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-017-51)  / 30 mL in 1 CUP, UNIT-DOSE (81033-017-30)", "package_ndc": "81033-017-51", "marketing_start_date": "20250401"}], "brand_name": "Sodium Citrate and Citric Acid", "product_id": "81033-017_334a40cd-5521-39e3-e063-6394a90ab024", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "81033-017", "generic_name": "Sodium Citrate and Citric Acid", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Citrate and Citric Acid", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "334 mg/5mL"}, {"name": "SODIUM CITRATE", "strength": "500 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}