Package 69918-301-30

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 69918-301-30
Digits Only 6991830130
Product NDC 69918-301
Product ID 69918-301_7bafece1-f0b8-4852-92ca-fe2bf261be04
Description

30 TABLET in 1 BOTTLE (69918-301-30)

Marketing

Marketing Status
Marketed Since 2016-03-01
Brand tranexamic acid
Generic tranexamic acid
Sample Package No

Linked Drug Pages (1)

Tranexamic Acid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7bafece1-f0b8-4852-92ca-fe2bf261be04", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["031bf7c2-3b07-469d-bc5a-31fc6238e25f"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Nordic Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69918-301-30)", "package_ndc": "69918-301-30", "marketing_start_date": "20160301"}], "brand_name": "Tranexamic Acid", "product_id": "69918-301_7bafece1-f0b8-4852-92ca-fe2bf261be04", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "69918-301", "generic_name": "Tranexamic Acid", "labeler_name": "Nordic Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranexamic Acid", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "650 mg/1"}], "application_number": "NDA022430", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160301", "listing_expiration_date": "20261231"}