Package 0409-1316-32

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 0409-1316-32
Digits Only 0409131632
Product NDC 0409-1316
Product ID 0409-1316_d77ce65b-d238-4187-aef4-593bc074d335
Description

50 CARTRIDGE in 1 CONTAINER (0409-1316-32) / .5 mL in 1 CARTRIDGE (0409-1316-11)

Marketing

Marketing Status
Marketed Since 2005-03-31
Brand heparin sodium
Generic heparin sodium
Sample Package No

Linked Drug Pages (1)

Heparin Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "d77ce65b-d238-4187-aef4-593bc074d335", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361853", "1659260"], "spl_set_id": ["c8c4edd2-ee9e-4558-6b8c-b83adc242a0a"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTRIDGE in 1 CONTAINER (0409-1316-32)  / .5 mL in 1 CARTRIDGE (0409-1316-11)", "package_ndc": "0409-1316-32", "marketing_start_date": "20050331"}], "brand_name": "Heparin Sodium", "product_id": "0409-1316_d77ce65b-d238-4187-aef4-593bc074d335", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-1316", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "10000 [USP'U]/mL"}], "application_number": "ANDA089522", "marketing_category": "ANDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}