Package 51662-1486-1
Brand: heparin sodium
Generic: heparin sodiumPackage Facts
Identity
Package NDC
51662-1486-1
Digits Only
5166214861
Product NDC
51662-1486
Description
1 mL in 1 VIAL, SINGLE-DOSE (51662-1486-1)
Marketing
Marketing Status
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": "34923afb-cdf0-1fc3-e063-6294a90a661c", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658637"], "spl_set_id": ["a07195bc-7442-32b4-e053-2995a90a0151"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1486-1)", "package_ndc": "51662-1486-1", "marketing_start_date": "20200309"}], "brand_name": "HEPARIN SODIUM", "product_id": "51662-1486_34923afb-cdf0-1fc3-e063-6294a90a661c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "51662-1486", "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": "10000 [USP'U]/mL"}], "application_number": "ANDA090571", "marketing_category": "ANDA", "marketing_start_date": "20200309", "listing_expiration_date": "20261231"}