Package 70518-4547-0

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4547-0
Digits Only 7051845470
Product NDC 70518-4547
Description

25 VIAL in 1 PACKAGE (70518-4547-0) / 1 mL in 1 VIAL (70518-4547-1)

Marketing

Marketing Status
Marketed Since 2026-01-16
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": "4885975b-67c0-5519-e063-6394a90a105b", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1659263"], "spl_set_id": ["a5fab0b1-c472-489c-ba87-2f8e53356173"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (70518-4547-0)  / 1 mL in 1 VIAL (70518-4547-1)", "package_ndc": "70518-4547-0", "marketing_start_date": "20260116"}], "brand_name": "Heparin Sodium", "product_id": "70518-4547_4885975b-67c0-5519-e063-6394a90a105b", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "70518-4547", "generic_name": "Heparin Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "NDA017037", "marketing_category": "NDA", "marketing_start_date": "20260116", "listing_expiration_date": "20271231"}