Package 71335-2695-3

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 71335-2695-3
Digits Only 7133526953
Product NDC 71335-2695
Description

4 TABLET in 1 BOTTLE (71335-2695-3)

Marketing

Marketing Status
Marketed Since 2025-09-24
Brand tranexamic acid
Generic tranexamic acid
Sample Package No

Linked Drug Pages (1)

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"}