Package 51662-1460-1

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 51662-1460-1
Digits Only 5166214601
Product NDC 51662-1460
Product ID 51662-1460_2b399ffc-9685-fbc4-e063-6294a90a3bf2
Description

1 mL in 1 CARTRIDGE (51662-1460-1)

Marketing

Marketing Status
Marketed Since 2019-12-22
Brand heparin sodium
Generic heparin sodium
Sample Package No

Linked Drug Pages (1)

HEPARIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2b399ffc-9685-fbc4-e063-6294a90a3bf2", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1659260"], "spl_set_id": ["9a5549ae-527a-1b83-e053-2a95a90a133d"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 CARTRIDGE (51662-1460-1)", "package_ndc": "51662-1460-1", "marketing_start_date": "20191222"}], "brand_name": "HEPARIN SODIUM", "product_id": "51662-1460_2b399ffc-9685-fbc4-e063-6294a90a3bf2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "51662-1460", "generic_name": "HEPARIN SODIUM", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HEPARIN SODIUM", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA088100", "marketing_category": "ANDA", "marketing_start_date": "20191222", "listing_expiration_date": "20261231"}