Package 0404-9872-01
Brand: heparin sodium
Generic: heparin sodiumPackage Facts
Identity
Package NDC
0404-9872-01
Digits Only
0404987201
Product NDC
0404-9872
Description
1 VIAL in 1 BAG (0404-9872-01) / 1 mL in 1 VIAL
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": "857a8443-d356-42b7-a0c1-c1a261e33b57", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1659263"], "spl_set_id": ["45dc6b8b-ed5d-40a2-8d9c-084c863ae93a"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9872-01) / 1 mL in 1 VIAL", "package_ndc": "0404-9872-01", "marketing_start_date": "20220111"}], "brand_name": "Heparin Sodium", "product_id": "0404-9872_857a8443-d356-42b7-a0c1-c1a261e33b57", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0404-9872", "generic_name": "Heparin Sodium", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA090808", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}