heparin sodium
Generic: heparin sodium
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 1000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-401
Product ID
25021-401_abc3d7f0-6a62-4542-bc8e-257f87322b93
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090810
Listing Expiration
2026-12-31
Marketing Start
2010-07-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021401
Hyphenated Format
25021-401
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
ANDA090810 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 [USP'U]/mL
Packaging
- 25 VIAL in 1 CARTON (25021-401-02) / 2 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "abc3d7f0-6a62-4542-bc8e-257f87322b93", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["6d5eae7d-a5f6-411c-b589-3e5f7eecc875"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-401-02) / 2 mL in 1 VIAL", "package_ndc": "25021-401-02", "marketing_start_date": "20100706"}], "brand_name": "Heparin Sodium", "product_id": "25021-401_abc3d7f0-6a62-4542-bc8e-257f87322b93", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "25021-401", "generic_name": "heparin sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA090810", "marketing_category": "ANDA", "marketing_start_date": "20100706", "listing_expiration_date": "20261231"}