heparin sodium
Generic: heparin sodium
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
mylan institutional llc
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 1000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67457-372
Product ID
67457-372_0aca9c58-9720-420b-a0fa-3ef6c841f35c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203851
Marketing Start
2018-05-25
Marketing End
2026-07-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67457372
Hyphenated Format
67457-372
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
ANDA203851 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 [USP'U]/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (67457-372-99) / 1 mL in 1 VIAL, SINGLE-DOSE (67457-372-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "0aca9c58-9720-420b-a0fa-3ef6c841f35c", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831"], "spl_set_id": ["88114716-5759-4bc9-8a85-d28da12962cc"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (67457-372-99) / 1 mL in 1 VIAL, SINGLE-DOSE (67457-372-12)", "package_ndc": "67457-372-99", "marketing_end_date": "20260731", "marketing_start_date": "20180525"}], "brand_name": "Heparin Sodium", "product_id": "67457-372_0aca9c58-9720-420b-a0fa-3ef6c841f35c", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "67457-372", "generic_name": "Heparin Sodium", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA203851", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20180525"}