heparin sodium

Generic: heparin sodium

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler northstar rxllc
Dosage Form INJECTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 20000 [USP'U]/mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-224
Product ID 72603-224_298bc179-9ab8-430f-9733-c33f7ea00d6e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211004
Listing Expiration 2026-12-31
Marketing Start 2024-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603224
Hyphenated Format 72603-224

Supplemental Identifiers

RxCUI
1361574
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 ANDA211004 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 20000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (72603-224-25) / 1 mL in 1 VIAL, MULTI-DOSE (72603-224-01)
source: ndc

Packages (1)

Ingredients (1)

heparin sodium (20000 [USP'U]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "298bc179-9ab8-430f-9733-c33f7ea00d6e", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361574"], "spl_set_id": ["34b8fe93-ee34-4a35-9af5-5d41705a28e9"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-224-25)  / 1 mL in 1 VIAL, MULTI-DOSE (72603-224-01)", "package_ndc": "72603-224-25", "marketing_start_date": "20240401"}], "brand_name": "Heparin Sodium", "product_id": "72603-224_298bc179-9ab8-430f-9733-c33f7ea00d6e", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-224", "generic_name": "Heparin Sodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "20000 [USP'U]/mL"}], "application_number": "ANDA211004", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}