Package 72572-255-25
Brand: heparin sodium
Generic: heparin sodiumPackage Facts
Identity
Package NDC
72572-255-25
Digits Only
7257225525
Product NDC
72572-255
Description
25 VIAL in 1 PACKAGE (72572-255-25) / 1 mL in 1 VIAL (72572-255-01)
Marketing
Marketing Status
Brand
heparin sodium
Generic
heparin sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "39ab19f4-c6c0-44b1-a082-6ffee418d184", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658659", "1659263"], "spl_set_id": ["1e362730-5a56-4948-a90f-2cb75fed9e91"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (72572-255-25) / 1 mL in 1 VIAL (72572-255-01)", "package_ndc": "72572-255-25", "marketing_start_date": "20191115"}], "brand_name": "Heparin Sodium", "product_id": "72572-255_39ab19f4-c6c0-44b1-a082-6ffee418d184", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72572-255", "generic_name": "Heparin Sodium", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "NDA017037", "marketing_category": "NDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}