Package 71288-401-02

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 71288-401-02
Digits Only 7128840102
Product NDC 71288-401
Description

25 VIAL, MULTI-DOSE in 1 CARTON (71288-401-02) / 1 mL in 1 VIAL, MULTI-DOSE (71288-401-01)

Marketing

Marketing Status
Marketed Since 2020-02-24
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": "154662b0-de60-4dcd-b92d-3401551b04db", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361574"], "spl_set_id": ["7df6c90c-3b55-4bb6-8a72-6e6a6aca4e7c"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (71288-401-02)  / 1 mL in 1 VIAL, MULTI-DOSE (71288-401-01)", "package_ndc": "71288-401-02", "marketing_start_date": "20200224"}], "brand_name": "Heparin Sodium", "product_id": "71288-401_154662b0-de60-4dcd-b92d-3401551b04db", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71288-401", "generic_name": "Heparin Sodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "20000 [USP'U]/mL"}], "application_number": "ANDA211004", "marketing_category": "ANDA", "marketing_start_date": "20200224", "listing_expiration_date": "20261231"}