Package 42571-314-89

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 42571-314-89
Digits Only 4257131489
Product NDC 42571-314
Description

10 CARTON in 1 CARTON (42571-314-89) / 1 VIAL, GLASS in 1 CARTON (42571-314-88) / 10 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2017-08-01
Brand tranexamic acid
Generic tranexamic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "45fc1537-9ab6-d1e9-e063-6394a90ab620", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["238720"], "spl_set_id": ["ee5aeb09-40fb-40f9-b655-97c50652a05e"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 CARTON (42571-314-89)  / 1 VIAL, GLASS in 1 CARTON (42571-314-88)  / 10 mL in 1 VIAL, GLASS", "package_ndc": "42571-314-89", "marketing_start_date": "20170801"}], "brand_name": "TRANEXAMIC ACID", "product_id": "42571-314_45fc1537-9ab6-d1e9-e063-6394a90ab620", "dosage_form": "INJECTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "42571-314", "generic_name": "TRANEXAMIC ACID", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "100 mg/mL"}], "application_number": "ANDA206713", "marketing_category": "ANDA", "marketing_start_date": "20170801", "listing_expiration_date": "20261231"}