heparin sodium

Generic: heparin sodium

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

Drug Facts

Product Profile

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

heparin sodium 200 [USP'U]/100mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-7620
Product ID 0409-7620_09688337-d13d-49c5-9235-a719ff77e8c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018916
Listing Expiration 2026-12-31
Marketing Start 2005-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04097620
Hyphenated Format 0409-7620

Supplemental Identifiers

RxCUI
1658690 1658692
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 NDA018916 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 [USP'U]/100mL
source: ndc
Packaging
  • 18 POUCH in 1 CASE (0409-7620-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-7620-13)
  • 12 POUCH in 1 CASE (0409-7620-59) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-7620-49)
source: ndc

Packages (2)

0409-7620-03 18 POUCH in 1 CASE (0409-7620-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-7620-13) 0409-7620-59 12 POUCH in 1 CASE (0409-7620-59) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-7620-49)

Ingredients (1)

heparin sodium (200 [USP'U]/100mL)

Linked Drug Pages (1)

Heparin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "09688337-d13d-49c5-9235-a719ff77e8c9", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658690", "1658692"], "spl_set_id": ["32e34077-aff1-4ec7-f9b0-b8e240768fb8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CASE (0409-7620-03)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-7620-13)", "package_ndc": "0409-7620-03", "marketing_start_date": "20050331"}, {"sample": false, "description": "12 POUCH in 1 CASE (0409-7620-59)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-7620-49)", "package_ndc": "0409-7620-59", "marketing_start_date": "20050331"}], "brand_name": "Heparin Sodium", "product_id": "0409-7620_09688337-d13d-49c5-9235-a719ff77e8c9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-7620", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "200 [USP'U]/100mL"}], "application_number": "NDA018916", "marketing_category": "NDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}