heparin sodium and dextrose

Generic: heparin sodium

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

Drug Facts

Product Profile

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

heparin sodium 10000 [USP'U]/100mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4520
Product ID 0409-4520_5a350331-f4ce-47bf-9f9e-f3c8083efc0c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019339
Listing Expiration 2026-12-31
Marketing Start 2022-12-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094520
Hyphenated Format 0409-4520

Supplemental Identifiers

RxCUI
1658717
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 and dextrose (source: ndc)
Generic Name heparin sodium (source: ndc)
Application Number NDA019339 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10000 [USP'U]/100mL
source: ndc
Packaging
  • 30 POUCH in 1 CASE (0409-4520-30) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-4520-02)
source: ndc

Packages (1)

Ingredients (1)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5a350331-f4ce-47bf-9f9e-f3c8083efc0c", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658717"], "spl_set_id": ["eede8a0c-5ae6-4166-84b3-12081405f08e"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CASE (0409-4520-30)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-4520-02)", "package_ndc": "0409-4520-30", "marketing_start_date": "20221212"}], "brand_name": "Heparin Sodium and Dextrose", "product_id": "0409-4520_5a350331-f4ce-47bf-9f9e-f3c8083efc0c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-4520", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium and Dextrose", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "10000 [USP'U]/100mL"}], "application_number": "NDA019339", "marketing_category": "NDA", "marketing_start_date": "20221212", "listing_expiration_date": "20261231"}