heparin sodium
Generic: heparin sodium
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
civica, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 1000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-250
Product ID
72572-250_39ab19f4-c6c0-44b1-a082-6ffee418d184
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017037
Listing Expiration
2026-12-31
Marketing Start
2019-11-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572250
Hyphenated Format
72572-250
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
NDA017037 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 [USP'U]/mL
Packaging
- 25 VIAL in 1 PACKAGE (72572-250-25) / 1 mL in 1 VIAL (72572-250-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "39ab19f4-c6c0-44b1-a082-6ffee418d184", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658659", "1659263"], "spl_set_id": ["1e362730-5a56-4948-a90f-2cb75fed9e91"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (72572-250-25) / 1 mL in 1 VIAL (72572-250-01)", "package_ndc": "72572-250-25", "marketing_start_date": "20191115"}], "brand_name": "Heparin Sodium", "product_id": "72572-250_39ab19f4-c6c0-44b1-a082-6ffee418d184", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72572-250", "generic_name": "Heparin Sodium", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "NDA017037", "marketing_category": "NDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}