tranexamic acid

Generic: tranexamic acid

Labeler: armas pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tranexamic acid
Generic Name tranexamic acid
Labeler armas pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

tranexamic acid 100 mg/mL

Manufacturer
Armas Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72485-107
Product ID 72485-107_49a3cee3-011b-4a23-a732-b5ec1c02c590
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206713
Listing Expiration 2026-12-31
Marketing Start 2021-06-11

Pharmacologic Class

Established (EPC)
antifibrinolytic agent [epc]
Physiologic Effect
decreased fibrinolysis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72485107
Hyphenated Format 72485-107

Supplemental Identifiers

UPC
0372485107018
UNII
6T84R30KC1
NUI
N0000175634 N0000175632

Packaging Origin

Original Packager
true

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 ANDA206713 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (72485-107-01) / 10 mL in 1 VIAL, GLASS
  • 10 VIAL, GLASS in 1 CARTON (72485-107-10) / 10 mL in 1 VIAL, GLASS
source: ndc

Packages (2)

Ingredients (1)

tranexamic acid (100 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "49a3cee3-011b-4a23-a732-b5ec1c02c590", "openfda": {"nui": ["N0000175634", "N0000175632"], "upc": ["0372485107018"], "unii": ["6T84R30KC1"], "spl_set_id": ["8d732fca-8157-49f9-9f08-acf9afb75aa2"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (72485-107-01)  / 10 mL in 1 VIAL, GLASS", "package_ndc": "72485-107-01", "marketing_start_date": "20210611"}, {"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (72485-107-10)  / 10 mL in 1 VIAL, GLASS", "package_ndc": "72485-107-10", "marketing_start_date": "20210611"}], "brand_name": "TRANEXAMIC ACID", "product_id": "72485-107_49a3cee3-011b-4a23-a732-b5ec1c02c590", "dosage_form": "INJECTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "72485-107", "generic_name": "TRANEXAMIC ACID", "labeler_name": "Armas Pharmaceuticals Inc.", "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": "20210611", "listing_expiration_date": "20261231"}