Package 72603-387-10

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 72603-387-10
Digits Only 7260338710
Product NDC 72603-387
Product ID 72603-387_8f780336-472e-45e4-9a62-9f1b938a44af
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (72603-387-10) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-387-01)

Marketing

Marketing Status
Marketed Since 2024-11-25
Brand tranexamic acid
Generic tranexamic acid
Sample Package No

Linked Drug Pages (1)

TRANEXAMIC ACID ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "8f780336-472e-45e4-9a62-9f1b938a44af", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["238720"], "spl_set_id": ["faa7c6bc-d7b9-48d5-9446-542a6a376db8"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72603-387-10)  / 10 mL in 1 VIAL, SINGLE-DOSE (72603-387-01)", "package_ndc": "72603-387-10", "marketing_start_date": "20241125"}], "brand_name": "TRANEXAMIC ACID", "product_id": "72603-387_8f780336-472e-45e4-9a62-9f1b938a44af", "dosage_form": "INJECTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "72603-387", "generic_name": "Tranexamic acid", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "100 mg/mL"}], "application_number": "ANDA203521", "marketing_category": "ANDA", "marketing_start_date": "20241125", "listing_expiration_date": "20261231"}