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 10000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-1316
Product ID
0409-1316_d77ce65b-d238-4187-aef4-593bc074d335
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089522
Listing Expiration
2026-12-31
Marketing Start
2005-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091316
Hyphenated Format
0409-1316
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
ANDA089522 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10000 [USP'U]/mL
Packaging
- 50 CARTRIDGE in 1 CONTAINER (0409-1316-32) / .5 mL in 1 CARTRIDGE (0409-1316-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "d77ce65b-d238-4187-aef4-593bc074d335", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361853", "1659260"], "spl_set_id": ["c8c4edd2-ee9e-4558-6b8c-b83adc242a0a"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTRIDGE in 1 CONTAINER (0409-1316-32) / .5 mL in 1 CARTRIDGE (0409-1316-11)", "package_ndc": "0409-1316-32", "marketing_start_date": "20050331"}], "brand_name": "Heparin Sodium", "product_id": "0409-1316_d77ce65b-d238-4187-aef4-593bc074d335", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0409-1316", "generic_name": "HEPARIN SODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "10000 [USP'U]/mL"}], "application_number": "ANDA089522", "marketing_category": "ANDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}