Package 83634-403-51

{"route": ["INTRAVENOUS"], "spl_id": "3de7c58b-1244-4ba9-af17-7a7f318e1255", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["2170286"], "spl_set_id": ["c3aad84a-aa99-42a0-b4b6-6fdee7585e19"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Avenacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (83634-403-51)  / 100 mL in 1 VIAL, SINGLE-DOSE (83634-403-82)", "package_ndc": "83634-403-51", "marketing_start_date": "20250901"}], "brand_name": "tranexamic acid in sodium chloride", "product_id": "83634-403_3de7c58b-1244-4ba9-af17-7a7f318e1255", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "83634-403", "generic_name": "tranexamic acid", "labeler_name": "Avenacy Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tranexamic acid in sodium chloride", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "10 mg/mL"}], "application_number": "ANDA218896", "marketing_category": "ANDA", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}