heparin sodium

Generic: heparin sodium

Labeler: civica, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler civica, inc.
Dosage Form INJECTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 1000 [USP'U]/mL

Manufacturer
Civica, Inc.

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
anti-coagulant [epc] heparin [cs] unfractionated heparin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572250
Hyphenated Format 72572-250

Supplemental Identifiers

RxCUI
1658659 1659263
UNII
ZZ45AB24CA

Packaging Origin

Original Packager
true

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
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL in 1 PACKAGE (72572-250-25) / 1 mL in 1 VIAL (72572-250-01)
source: ndc

Packages (1)

Ingredients (1)

heparin sodium (1000 [USP'U]/mL)

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"}