Package 0121-0677-16

{"route": ["ORAL"], "spl_id": "3082f36b-0006-4aee-9019-38995d2292fd", "openfda": {"upc": ["0301210677168"], "unii": ["2968PHW8QP", "EE90ONI6FF", "1Q73Q2JULR"], "rxcui": ["309317"], "spl_set_id": ["2ecb42a2-82f1-456b-8f1e-02c2d0a7b5ad"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-0677-16)", "package_ndc": "0121-0677-16", "marketing_start_date": "20050525"}], "brand_name": "TRICITRATES", "product_id": "0121-0677_3082f36b-0006-4aee-9019-38995d2292fd", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0121-0677", "generic_name": "POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRICITRATES", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "334 mg/5mL"}, {"name": "POTASSIUM CITRATE", "strength": "550 mg/5mL"}, {"name": "SODIUM CITRATE", "strength": "500 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20050525", "listing_expiration_date": "20261231"}