Package 63629-8838-1

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 63629-8838-1
Digits Only 6362988381
Product NDC 63629-8838
Description

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

Marketing

Marketing Status
Marketed Since 2021-09-10
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": "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"}