Package 72603-336-25

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 72603-336-25
Digits Only 7260333625
Product NDC 72603-336
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (72603-336-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)

Marketing

Marketing Status
Marketed Since 2024-04-01
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": "aa6e8c00-0911-4b53-9b2c-c3130bccfdcd", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["41dd053d-49f6-4eb1-b9e7-3508ede82df8"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72603-336-25)  / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)", "package_ndc": "72603-336-25", "marketing_start_date": "20240401"}], "brand_name": "Heparin Sodium", "product_id": "72603-336_aa6e8c00-0911-4b53-9b2c-c3130bccfdcd", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-336", "generic_name": "Heparin Sodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "2000 [USP'U]/2mL"}], "application_number": "ANDA211005", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}