heparin sodium and dextrose
Generic: heparin sodium
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
heparin sodium and dextrose
Generic Name
heparin sodium
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 10000 [USP'U]/100mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094520
Hyphenated Format
0409-4520
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10000 [USP'U]/100mL
Packaging
- 30 POUCH in 1 CASE (0409-4520-30) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-4520-02)
Packages (1)
Ingredients (1)
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"}