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 1000 [USP'U]/mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-234
Product ID 72603-234_99ddee9d-4b78-4729-a69e-d859be6df0ae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211007
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 72603234
Hyphenated Format 72603-234

Supplemental Identifiers

RxCUI
1361226 1361615 1658637 1658659 1659263
UPC
0372603412253
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 ANDA211007 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (72603-234-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72603-234-01)
source: ndc

Packages (1)

72603-234-25 25 VIAL, SINGLE-DOSE in 1 CARTON (72603-234-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72603-234-01)

Ingredients (1)

heparin sodium (1000 [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": "99ddee9d-4b78-4729-a69e-d859be6df0ae", "openfda": {"upc": ["0372603412253"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1658637", "1658659", "1659263"], "spl_set_id": ["c4fa6d34-e76b-4c3c-b74d-21ce41432a04"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72603-234-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (72603-234-01)", "package_ndc": "72603-234-25", "marketing_start_date": "20240401"}], "brand_name": "Heparin Sodium", "product_id": "72603-234_99ddee9d-4b78-4729-a69e-d859be6df0ae", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-234", "generic_name": "Heparin Sodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA211007", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}