Package 51754-0108-1

{"route": ["INTRAVENOUS"], "spl_id": "0ae0a575-08e1-43a3-9b6c-8c5f165db35f", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["2170286"], "spl_set_id": ["db36ddf2-4ac5-47ac-bdce-e3fa6983073e"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BAG (51754-0108-1)", "package_ndc": "51754-0108-1", "marketing_start_date": "20190601"}, {"sample": false, "description": "1000 mL in 1 CASE (51754-0108-3)", "package_ndc": "51754-0108-3", "marketing_start_date": "20190601"}], "brand_name": "TRANEXAMIC ACID IN SODIUM CHLORIDE", "product_id": "51754-0108_0ae0a575-08e1-43a3-9b6c-8c5f165db35f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "51754-0108", "generic_name": "tranexamic acid", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID IN SODIUM CHLORIDE", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "10 mg/mL"}], "application_number": "NDA212020", "marketing_category": "NDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}