heparin sodium

Generic: heparin sodium

Labeler: sagent pharmaceticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler sagent pharmaceticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 5000 [USP'U]/mL

Manufacturer
Sagent Pharmaceticals

Identifiers & Regulatory

Product NDC 25021-402
Product ID 25021-402_b44c59b9-34b9-4244-90a8-928c20ad1e84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090808
Listing Expiration 2026-12-31
Marketing Start 2014-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021402
Hyphenated Format 25021-402

Supplemental Identifiers

RxCUI
1361226 1361615 1362831
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 ANDA090808 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 5000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-402-66) / 1 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

heparin sodium (5000 [USP'U]/mL)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "b44c59b9-34b9-4244-90a8-928c20ad1e84", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831"], "spl_set_id": ["ef309d83-7262-4874-8580-f4ca254f963a"], "manufacturer_name": ["Sagent Pharmaceticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-402-66)  / 1 mL in 1 VIAL", "package_ndc": "25021-402-66", "marketing_start_date": "20140701"}], "brand_name": "Heparin Sodium", "product_id": "25021-402_b44c59b9-34b9-4244-90a8-928c20ad1e84", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "25021-402", "generic_name": "Heparin Sodium", "labeler_name": "Sagent Pharmaceticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA090808", "marketing_category": "ANDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}