tranexamic acid
Generic: tranexamic acid
Labeler: nexus pharmaceuticals llcDrug Facts
Product Profile
Brand Name
tranexamic acid
Generic Name
tranexamic acid
Labeler
nexus pharmaceuticals llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
tranexamic acid 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
14789-115
Product ID
14789-115_2f0e80ab-c6c5-cb03-e063-6394a90a1f92
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216877
Listing Expiration
2026-12-31
Marketing Start
2024-06-25
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
14789115
Hyphenated Format
14789-115
Supplemental Identifiers
RxCUI
UPC
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
ANDA216877 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 BAG in 1 CARTON (14789-115-05) / 100 mL in 1 BAG (14789-115-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2f0e80ab-c6c5-cb03-e063-6394a90a1f92", "openfda": {"nui": ["N0000175634", "N0000175632"], "upc": ["0314789115085"], "unii": ["6T84R30KC1"], "rxcui": ["2170286"], "spl_set_id": ["c479dccd-15c6-47c2-9675-680ebb9db2cb"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CARTON (14789-115-05) / 100 mL in 1 BAG (14789-115-08)", "package_ndc": "14789-115-05", "marketing_start_date": "20240625"}], "brand_name": "Tranexamic Acid", "product_id": "14789-115_2f0e80ab-c6c5-cb03-e063-6394a90a1f92", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "14789-115", "generic_name": "Tranexamic Acid", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranexamic Acid", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "10 mg/mL"}], "application_number": "ANDA216877", "marketing_category": "ANDA", "marketing_start_date": "20240625", "listing_expiration_date": "20261231"}