Package 0409-1005-20

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 0409-1005-20
Digits Only 0409100520
Product NDC 0409-1005
Description

20 POUCH in 1 CASE (0409-1005-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-1005-01)

Marketing

Marketing Status
Marketed Since 2023-02-27
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"], "spl_id": "09688337-d13d-49c5-9235-a719ff77e8c9", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658690", "1658692"], "spl_set_id": ["32e34077-aff1-4ec7-f9b0-b8e240768fb8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 POUCH in 1 CASE (0409-1005-20)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-1005-01)", "package_ndc": "0409-1005-20", "marketing_start_date": "20230227"}], "brand_name": "Heparin Sodium", "product_id": "0409-1005_09688337-d13d-49c5-9235-a719ff77e8c9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-1005", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "200 [USP'U]/100mL"}], "application_number": "NDA018916", "marketing_category": "NDA", "marketing_start_date": "20230227", "listing_expiration_date": "20261231"}