heparin sodium
Generic: heparin sodium
Labeler: sagent pharmaceticalsDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
sagent pharmaceticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 5000 [USP'U]/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021402
Hyphenated Format
25021-402
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
ANDA090808 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5000 [USP'U]/mL
Packaging
- 25 VIAL in 1 CARTON (25021-402-66) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
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"}