heparin sodium

Generic: heparin sodium

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 5000 [USP'U]/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1460
Product ID 51662-1460_2b399ffc-9685-fbc4-e063-6294a90a3bf2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088100
Listing Expiration 2026-12-31
Marketing Start 2019-12-22

Pharmacologic Class

Classes
anti-coagulant [epc] heparin [cs] unfractionated heparin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621460
Hyphenated Format 51662-1460

Supplemental Identifiers

RxCUI
1659260
UNII
ZZ45AB24CA

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name heparin sodium (source: ndc)
Generic Name heparin sodium (source: ndc)
Application Number ANDA088100 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 5000 [USP'U]/mL
source: ndc
Packaging
  • 1 mL in 1 CARTRIDGE (51662-1460-1)
source: ndc

Packages (1)

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

Ingredients (1)

heparin sodium (5000 [USP'U]/mL)

Linked Drug Pages (1)

HEPARIN SODIUM ndc-match (0.9)

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"}