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 2000 [USP'U]/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-336
Product ID
72603-336_aa6e8c00-0911-4b53-9b2c-c3130bccfdcd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211005
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
72603336
Hyphenated Format
72603-336
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
ANDA211005 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2000 [USP'U]/2mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (72603-336-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "aa6e8c00-0911-4b53-9b2c-c3130bccfdcd", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["41dd053d-49f6-4eb1-b9e7-3508ede82df8"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72603-336-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)", "package_ndc": "72603-336-25", "marketing_start_date": "20240401"}], "brand_name": "Heparin Sodium", "product_id": "72603-336_aa6e8c00-0911-4b53-9b2c-c3130bccfdcd", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "72603-336", "generic_name": "Heparin Sodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "2000 [USP'U]/2mL"}], "application_number": "ANDA211005", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}