heparin sodium
Generic: heparin sodium
Labeler: northstar rxllcDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
northstar rxllc
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 20000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-224
Product ID
72603-224_298bc179-9ab8-430f-9733-c33f7ea00d6e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211004
Listing Expiration
2026-12-31
Marketing Start
2024-04-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603224
Hyphenated Format
72603-224
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
ANDA211004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20000 [USP'U]/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 CARTON (72603-224-25) / 1 mL in 1 VIAL, MULTI-DOSE (72603-224-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "298bc179-9ab8-430f-9733-c33f7ea00d6e", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361574"], "spl_set_id": ["34b8fe93-ee34-4a35-9af5-5d41705a28e9"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-224-25) / 1 mL in 1 VIAL, MULTI-DOSE (72603-224-01)", "package_ndc": "72603-224-25", "marketing_start_date": "20240401"}], "brand_name": "Heparin Sodium", "product_id": "72603-224_298bc179-9ab8-430f-9733-c33f7ea00d6e", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-224", "generic_name": "Heparin Sodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "20000 [USP'U]/mL"}], "application_number": "ANDA211004", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}