tranexamic acid
Generic: tranexamic acid
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
tranexamic acid
Generic Name
tranexamic acid
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
tranexamic acid 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-418
Product ID
25021-418_c81489bf-115d-4b9c-a24d-596d0cd53c84
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218599
Listing Expiration
2026-12-31
Marketing Start
2024-09-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021418
Hyphenated Format
25021-418
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
tranexamic acid (source: ndc)
Generic Name
tranexamic acid (source: ndc)
Application Number
ANDA218599 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 BAG in 1 CARTON (25021-418-82) / 100 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c81489bf-115d-4b9c-a24d-596d0cd53c84", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["2170286"], "spl_set_id": ["80465b90-3f92-4e35-b2ba-69871bbd4a7f"], "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 BAG in 1 CARTON (25021-418-82) / 100 mL in 1 BAG", "package_ndc": "25021-418-82", "marketing_start_date": "20240915"}], "brand_name": "Tranexamic Acid", "product_id": "25021-418_c81489bf-115d-4b9c-a24d-596d0cd53c84", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "25021-418", "generic_name": "Tranexamic Acid", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranexamic Acid", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "10 mg/mL"}], "application_number": "ANDA218599", "marketing_category": "ANDA", "marketing_start_date": "20240915", "listing_expiration_date": "20261231"}