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, FILM COATED
Routes
ORAL
Active Ingredients

tranexamic acid 650 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8838
Product ID 63629-8838_30e26790-6561-4a6a-938c-67ce81739ba2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202093
Listing Expiration 2026-12-31
Marketing Start 2013-01-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636298838
Hyphenated Format 63629-8838

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 ANDA202093 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-8838-1)
source: ndc

Packages (1)

63629-8838-1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-8838-1)

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": "30e26790-6561-4a6a-938c-67ce81739ba2", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["128c39ce-f625-47ec-9efe-4de696e5220f"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-8838-1)", "package_ndc": "63629-8838-1", "marketing_start_date": "20210910"}], "brand_name": "Tranexamic Acid", "product_id": "63629-8838_30e26790-6561-4a6a-938c-67ce81739ba2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "63629-8838", "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": "ANDA202093", "marketing_category": "ANDA", "marketing_start_date": "20130103", "listing_expiration_date": "20261231"}