Package 25021-401-02

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 25021-401-02
Digits Only 2502140102
Product NDC 25021-401
Product ID 25021-401_abc3d7f0-6a62-4542-bc8e-257f87322b93
Description

25 VIAL in 1 CARTON (25021-401-02) / 2 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": "abc3d7f0-6a62-4542-bc8e-257f87322b93", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["6d5eae7d-a5f6-411c-b589-3e5f7eecc875"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-401-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-401-02", "marketing_start_date": "20100706"}], "brand_name": "Heparin Sodium", "product_id": "25021-401_abc3d7f0-6a62-4542-bc8e-257f87322b93", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "25021-401", "generic_name": "heparin sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA090810", "marketing_category": "ANDA", "marketing_start_date": "20100706", "listing_expiration_date": "20261231"}