Package 0121-0595-16
Brand: sodium citrate and citric acid
Generic: sodium citrate and citric acid monohydratePackage Facts
Identity
Package NDC
0121-0595-16
Digits Only
0121059516
Product NDC
0121-0595
Description
473 mL in 1 BOTTLE (0121-0595-16)
Marketing
Marketing Status
Brand
sodium citrate and citric acid
Generic
sodium citrate and citric acid monohydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26ce1be6-a69a-63f8-e063-6394a90ad637", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["1Q73Q2JULR", "XF417D3PSL"], "rxcui": ["543014"], "spl_set_id": ["63201a61-6ac5-41ae-8b2d-ff0d3a8ddfd5"], "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": ["Pharmaceutical Associates, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-0595-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-0595-15)", "package_ndc": "0121-0595-00", "marketing_start_date": "19690101"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0121-0595-16)", "package_ndc": "0121-0595-16", "marketing_start_date": "19690101"}, {"sample": false, "description": "10 TRAY in 1 CASE (0121-0595-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-0595-30", "marketing_start_date": "19690101"}], "brand_name": "Sodium Citrate and Citric Acid", "product_id": "0121-0595_26ce1be6-a69a-63f8-e063-6394a90ad637", "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": "0121-0595", "generic_name": "SODIUM CITRATE and CITRIC ACID MONOHYDRATE", "labeler_name": "Pharmaceutical Associates, Inc.", "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": "19690101", "listing_expiration_date": "20261231"}