Package 51662-1578-1

Brand: heparin sodium in sodium chloride

Generic: heparin sodium in sodium chloride
NDC Package

Package Facts

Identity

Package NDC 51662-1578-1
Digits Only 5166215781
Product NDC 51662-1578
Product ID 51662-1578_0ff8e2fb-b791-dd77-e063-6294a90ab4ea
Description

250 mL in 1 BAG (51662-1578-1)

Marketing

Marketing Status
Marketed Since 2021-07-15
Brand heparin sodium in sodium chloride
Generic heparin sodium in sodium chloride
Sample Package No

Linked Drug Pages (1)

HEPARIN SODIUM IN SODIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0ff8e2fb-b791-dd77-e063-6294a90ab4ea", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658717"], "spl_set_id": ["c72b193e-0687-e002-e053-2995a90a7182"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1578-1)", "package_ndc": "51662-1578-1", "marketing_start_date": "20210715"}], "brand_name": "HEPARIN SODIUM IN SODIUM CHLORIDE", "product_id": "51662-1578_0ff8e2fb-b791-dd77-e063-6294a90ab4ea", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "51662-1578", "generic_name": "HEPARIN SODIUM IN SODIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HEPARIN SODIUM IN SODIUM CHLORIDE", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "10000 [USP'U]/100mL"}], "application_number": "NDA017029", "marketing_category": "NDA", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}