Package 25021-415-66

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 25021-415-66
Digits Only 2502141566
Product NDC 25021-415
Description

10 VIAL in 1 CARTON (25021-415-66) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-10-15
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": "bdcdab6a-42b4-4f10-b751-5552e9b331cc", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["238720"], "spl_set_id": ["b28a18a4-391d-48ab-8fa5-6391f15553f3"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-415-66)  / 10 mL in 1 VIAL", "package_ndc": "25021-415-66", "marketing_start_date": "20251015"}], "brand_name": "Tranexamic Acid", "product_id": "25021-415_bdcdab6a-42b4-4f10-b751-5552e9b331cc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "25021-415", "generic_name": "Tranexamic Acid", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranexamic Acid", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "100 mg/mL"}], "application_number": "ANDA207239", "marketing_category": "ANDA", "marketing_start_date": "20251015", "listing_expiration_date": "20261231"}