heparin sodium
Generic: heparin sodium
Labeler: phlow corporationDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
phlow corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 1000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
81565-203
Product ID
81565-203_4bebb181-0ed2-44b0-af0d-4802862e73b4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017029
Listing Expiration
2026-12-31
Marketing Start
2022-03-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81565203
Hyphenated Format
81565-203
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 in 1 TRAY (81565-203-02) / 10 mL in 1 VIAL (81565-203-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4bebb181-0ed2-44b0-af0d-4802862e73b4", "openfda": {"upc": ["0381565203014"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226"], "spl_set_id": ["cece935c-1c0a-4949-b023-d6df3d53fbfa"], "manufacturer_name": ["Phlow Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (81565-203-02) / 10 mL in 1 VIAL (81565-203-01)", "package_ndc": "81565-203-02", "marketing_start_date": "20220307"}], "brand_name": "Heparin Sodium", "product_id": "81565-203_4bebb181-0ed2-44b0-af0d-4802862e73b4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "81565-203", "generic_name": "HEPARIN SODIUM", "labeler_name": "Phlow Corporation", "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": "20220307", "listing_expiration_date": "20261231"}