Package 25021-404-01

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 25021-404-01
Digits Only 2502140401
Product NDC 25021-404
Product ID 25021-404_bb6d321d-a569-4736-88a0-c979074d71ef
Description

25 VIAL in 1 CARTON (25021-404-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2010-07-06
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": "bb6d321d-a569-4736-88a0-c979074d71ef", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361574"], "spl_set_id": ["feec2820-502f-4a97-84c9-f173729c51d3"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-404-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-404-01", "marketing_start_date": "20100706"}], "brand_name": "Heparin Sodium", "product_id": "25021-404_bb6d321d-a569-4736-88a0-c979074d71ef", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "25021-404", "generic_name": "heparin sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "20000 [USP'U]/mL"}], "application_number": "ANDA090809", "marketing_category": "ANDA", "marketing_start_date": "20100706", "listing_expiration_date": "20261231"}