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 1000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-540
Product ID
63323-540_df982e37-d056-462a-9df5-2105e16504d2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017029
Listing Expiration
2026-12-31
Marketing Start
1972-02-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323540
Hyphenated Format
63323-540
Supplemental Identifiers
RxCUI
UPC
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
- 1000 [USP'U]/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 TRAY (63323-540-67) / 10 mL in 1 VIAL, MULTI-DOSE (63323-540-07)
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "df982e37-d056-462a-9df5-2105e16504d2", "openfda": {"upc": ["0363323540074", "0363323262099"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615"], "spl_set_id": ["ed937dd2-8fab-4875-a1e8-627b71ccb7fb"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-540-67) / 10 mL in 1 VIAL, MULTI-DOSE (63323-540-07)", "package_ndc": "63323-540-67", "marketing_start_date": "20200325"}], "brand_name": "Heparin Sodium", "product_id": "63323-540_df982e37-d056-462a-9df5-2105e16504d2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "63323-540", "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": "1000 [USP'U]/mL"}], "application_number": "NDA017029", "marketing_category": "NDA", "marketing_start_date": "19720222", "listing_expiration_date": "20261231"}