Package 0409-1402-12
Brand: heparin sodium
Generic: heparin sodiumPackage Facts
Identity
Package NDC
0409-1402-12
Digits Only
0409140212
Product NDC
0409-1402
Description
50 CARTRIDGE in 1 BOX (0409-1402-12) / 1 mL in 1 CARTRIDGE (0409-1402-27)
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": "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 BOX (0409-1402-12) / 1 mL in 1 CARTRIDGE (0409-1402-27)", "package_ndc": "0409-1402-12", "marketing_start_date": "20110218"}], "brand_name": "Heparin Sodium", "product_id": "0409-1402_d77ce65b-d238-4187-aef4-593bc074d335", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-1402", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA088100", "marketing_category": "ANDA", "marketing_start_date": "20110218", "listing_expiration_date": "20261231"}