heparin sodium

Generic: heparin sodium

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler northstar rx llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 5000 [USP'U]/mL

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-456
Product ID 72603-456_2edf6d47-aa94-af01-e063-6394a90a5c01
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202957
Listing Expiration 2026-12-31
Marketing Start 2014-06-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603456
Hyphenated Format 72603-456

Supplemental Identifiers

RxCUI
1361226 1361615 1362831
UPC
0372603456011 0372603250251 0372603250015 0372603579017 0372603579253 0372603456257
UNII
ZZ45AB24CA

Packaging Origin

Original Packager
true

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 ANDA202957 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 5000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (72603-456-25) / 1 mL in 1 VIAL, MULTI-DOSE (72603-456-01)
source: ndc

Packages (1)

Ingredients (1)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2edf6d47-aa94-af01-e063-6394a90a5c01", "openfda": {"upc": ["0372603456011", "0372603250251", "0372603250015", "0372603579017", "0372603579253", "0372603456257"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831"], "spl_set_id": ["2edf6d35-5cf3-b7ff-e063-6394a90a4f33"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-456-25)  / 1 mL in 1 VIAL, MULTI-DOSE (72603-456-01)", "package_ndc": "72603-456-25", "marketing_start_date": "20250301"}], "brand_name": "Heparin Sodium", "product_id": "72603-456_2edf6d47-aa94-af01-e063-6394a90a5c01", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-456", "generic_name": "Heparin Sodium", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA202957", "marketing_category": "ANDA", "marketing_start_date": "20140612", "listing_expiration_date": "20261231"}