heparin sodium

Generic: heparin sodium

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 1000 [USP'U]/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-2720
Product ID 0409-2720_810760c7-a209-4cd1-ae0e-462cd2a95bf6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090571
Listing Expiration 2026-12-31
Marketing Start 2009-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04092720
Hyphenated Format 0409-2720

Supplemental Identifiers

RxCUI
1361226 1361615 1658637 1658659 1659263
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 ANDA090571 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-2720-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-2720-30)
  • 25 VIAL, MULTI-DOSE in 1 TRAY (0409-2720-02) / 10 mL in 1 VIAL, MULTI-DOSE (0409-2720-31)
  • 25 VIAL, MULTI-DOSE in 1 TRAY (0409-2720-03) / 30 mL in 1 VIAL, MULTI-DOSE (0409-2720-32)
source: ndc

Packages (3)

Ingredients (1)

heparin sodium (1000 [USP'U]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "810760c7-a209-4cd1-ae0e-462cd2a95bf6", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1658637", "1658659", "1659263"], "spl_set_id": ["6c181d7e-aed2-4975-30ac-d39a94cca7ec"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-2720-01)  / 1 mL in 1 VIAL, SINGLE-DOSE (0409-2720-30)", "package_ndc": "0409-2720-01", "marketing_start_date": "20090831"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-2720-02)  / 10 mL in 1 VIAL, MULTI-DOSE (0409-2720-31)", "package_ndc": "0409-2720-02", "marketing_start_date": "20090831"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-2720-03)  / 30 mL in 1 VIAL, MULTI-DOSE (0409-2720-32)", "package_ndc": "0409-2720-03", "marketing_start_date": "20090831"}], "brand_name": "Heparin Sodium", "product_id": "0409-2720_810760c7-a209-4cd1-ae0e-462cd2a95bf6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-2720", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA090571", "marketing_category": "ANDA", "marketing_start_date": "20090831", "listing_expiration_date": "20261231"}