heparin sodium
Generic: heparin sodium
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 5000 [USP'U]/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-3150
Product ID
0409-3150_6f12c416-7979-41c0-b7d7-e198aa0cad8a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018916
Listing Expiration
2026-12-31
Marketing Start
2023-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04093150
Hyphenated Format
0409-3150
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 (source: ndc)
Generic Name
heparin sodium (source: ndc)
Application Number
NDA018916 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5000 [USP'U]/100mL
Packaging
- 20 POUCH in 1 CASE (0409-3150-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-3150-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6f12c416-7979-41c0-b7d7-e198aa0cad8a", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658717", "1659195", "1659196", "1659197"], "spl_set_id": ["0413f511-6b34-4c15-e48b-3fad08baacbe"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 POUCH in 1 CASE (0409-3150-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-3150-05)", "package_ndc": "0409-3150-20", "marketing_start_date": "20230103"}], "brand_name": "Heparin Sodium", "product_id": "0409-3150_6f12c416-7979-41c0-b7d7-e198aa0cad8a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-3150", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/100mL"}], "application_number": "NDA018916", "marketing_category": "NDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}