tranexamic acid

Generic: tranexamic acid

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tranexamic acid
Generic Name tranexamic acid
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tranexamic acid 650 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2695
Product ID 71335-2695_c616ecfa-42f7-49a2-898f-5aee4405c607
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218320
Listing Expiration 2026-12-31
Marketing Start 2024-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352695
Hyphenated Format 71335-2695

Supplemental Identifiers

RxCUI
883826
UNII
6T84R30KC1
NUI
N0000175634 N0000175632

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 ANDA218320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 8 TABLET in 1 BOTTLE (71335-2695-1)
  • 30 TABLET in 1 BOTTLE (71335-2695-2)
  • 4 TABLET in 1 BOTTLE (71335-2695-3)
source: ndc

Packages (3)

71335-2695-1 8 TABLET in 1 BOTTLE (71335-2695-1) 71335-2695-2 30 TABLET in 1 BOTTLE (71335-2695-2) 71335-2695-3 4 TABLET in 1 BOTTLE (71335-2695-3)

Ingredients (1)

tranexamic acid (650 mg/1)

Linked Drug Pages (1)

TRANEXAMIC ACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c616ecfa-42f7-49a2-898f-5aee4405c607", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["5b0c13fe-2c8e-4ac8-8bda-140881bd0cc4"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE (71335-2695-1)", "package_ndc": "71335-2695-1", "marketing_start_date": "20250924"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2695-2)", "package_ndc": "71335-2695-2", "marketing_start_date": "20250924"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE (71335-2695-3)", "package_ndc": "71335-2695-3", "marketing_start_date": "20250924"}], "brand_name": "TRANEXAMIC ACID", "product_id": "71335-2695_c616ecfa-42f7-49a2-898f-5aee4405c607", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "71335-2695", "generic_name": "TRANEXAMIC ACID", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "650 mg/1"}], "application_number": "ANDA218320", "marketing_category": "ANDA", "marketing_start_date": "20240611", "listing_expiration_date": "20261231"}