Package 71872-7351-1

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 71872-7351-1
Digits Only 7187273511
Product NDC 71872-7351
Description

1 VIAL, MULTI-DOSE in 1 BAG (71872-7351-1) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2025-05-07
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": "3ea2be5c-3695-7da1-e063-6294a90af80c", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226"], "spl_set_id": ["3ea2bd53-ed13-a516-e063-6394a90a5dd9"], "manufacturer_name": ["Medical Purchasing Solutions, LLC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7351-1)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7351-1", "marketing_start_date": "20250507"}], "brand_name": "Heparin Sodium", "product_id": "71872-7351_3ea2be5c-3695-7da1-e063-6294a90af80c", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71872-7351", "generic_name": "Heparin Sodium", "labeler_name": "Medical Purchasing Solutions, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA211007", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}