Package 51662-1532-1

Brand: tranexamic acid

Generic: tranexamic acid
NDC Package

Package Facts

Identity

Package NDC 51662-1532-1
Digits Only 5166215321
Product NDC 51662-1532
Description

10 mL in 1 VIAL, SINGLE-DOSE (51662-1532-1)

Marketing

Marketing Status
Marketed Since 2021-06-20
Brand tranexamic acid
Generic tranexamic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1035853c-6cb9-76b2-e063-6394a90a3938", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["238720"], "spl_set_id": ["c53e2b38-6c49-acae-e053-2995a90ae9df"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1532-1)", "package_ndc": "51662-1532-1", "marketing_start_date": "20210620"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1532-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1532-2)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1532-3", "marketing_start_date": "20210620"}], "brand_name": "TRANEXAMIC ACID", "product_id": "51662-1532_1035853c-6cb9-76b2-e063-6394a90a3938", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "51662-1532", "generic_name": "TRANEXAMIC ACID", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "100 mg/mL"}], "application_number": "ANDA205035", "marketing_category": "ANDA", "marketing_start_date": "20210620", "listing_expiration_date": "20261231"}