Package 67457-384-99

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 67457-384-99
Digits Only 6745738499
Product NDC 67457-384
Description

25 VIAL, MULTI-DOSE in 1 CARTON (67457-384-99) / 30 mL in 1 VIAL, MULTI-DOSE (67457-384-31)

Marketing

Marketing Status
Discontinued 2026-09-30
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": "0aca9c58-9720-420b-a0fa-3ef6c841f35c", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831"], "spl_set_id": ["88114716-5759-4bc9-8a85-d28da12962cc"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (67457-384-99)  / 30 mL in 1 VIAL, MULTI-DOSE (67457-384-31)", "package_ndc": "67457-384-99", "marketing_end_date": "20260930", "marketing_start_date": "20180316"}], "brand_name": "Heparin Sodium", "product_id": "67457-384_0aca9c58-9720-420b-a0fa-3ef6c841f35c", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "67457-384", "generic_name": "Heparin Sodium", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA203851", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20180316"}