Package 63629-8599-1

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 63629-8599-1
Digits Only 6362985991
Product NDC 63629-8599
Description

8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-8599-1)

Marketing

Marketing Status
Marketed Since 2021-06-28
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": "8d9c163d-5a47-4c45-98bf-b9a59813542a", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["4ddba10f-705a-40af-83b8-aa1fd68891f8"], "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, FILM COATED in 1 BOTTLE, PLASTIC (63629-8599-1)", "package_ndc": "63629-8599-1", "marketing_start_date": "20210628"}], "brand_name": "Tranexamic Acid", "product_id": "63629-8599_8d9c163d-5a47-4c45-98bf-b9a59813542a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "63629-8599", "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"}