heparin sodium in sodium chloride

Generic: heparin sodium in sodium chloride

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

Drug Facts

Product Profile

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

heparin sodium 10000 [USP'U]/100mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1578
Product ID 51662-1578_0ff8e2fb-b791-dd77-e063-6294a90ab4ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017029
Listing Expiration 2026-12-31
Marketing Start 2021-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621578
Hyphenated Format 51662-1578

Supplemental Identifiers

RxCUI
1658717
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 in sodium chloride (source: ndc)
Generic Name heparin sodium in sodium chloride (source: ndc)
Application Number NDA017029 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10000 [USP'U]/100mL
source: ndc
Packaging
  • 250 mL in 1 BAG (51662-1578-1)
source: ndc

Packages (1)

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

Ingredients (1)

heparin sodium (10000 [USP'U]/100mL)

Linked Drug Pages (1)

HEPARIN SODIUM IN SODIUM CHLORIDE ndc-match (0.9)

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"}