heparin sodium
Generic: heparin sodium
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 5000 [USP'U]/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-522
Product ID
63323-522_c656be9f-793a-4d25-b563-539dce89cbc0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017029
Listing Expiration
2026-12-31
Marketing Start
2017-08-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323522
Hyphenated Format
63323-522
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
NDA017029 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5000 [USP'U]/100mL
Packaging
- 24 BAG in 1 CASE (63323-522-77) / 500 mL in 1 BAG (63323-522-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c656be9f-793a-4d25-b563-539dce89cbc0", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658717", "1659195"], "spl_set_id": ["cb1c1e7a-c9ca-4a07-8833-e45ce436d287"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CASE (63323-522-77) / 500 mL in 1 BAG (63323-522-01)", "package_ndc": "63323-522-77", "marketing_start_date": "20170824"}], "brand_name": "Heparin Sodium", "product_id": "63323-522_c656be9f-793a-4d25-b563-539dce89cbc0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "63323-522", "generic_name": "HEPARIN SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/100mL"}], "application_number": "NDA017029", "marketing_category": "NDA", "marketing_start_date": "20170824", "listing_expiration_date": "20261231"}