ferabright
Generic: ferumoxytol
Labeler: azurity pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ferabright
Generic Name
ferumoxytol
Labeler
azurity pharmaceuticals, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ferumoxytol 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24338-310
Product ID
24338-310_ac5e7507-8e66-4da5-abd9-75ae80369b9f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA219868
Listing Expiration
2026-12-31
Marketing Start
2025-10-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24338310
Hyphenated Format
24338-310
Supplemental Identifiers
UPC
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
ferabright (source: ndc)
Generic Name
ferumoxytol (source: ndc)
Application Number
NDA219868 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (24338-310-10) / 10 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ac5e7507-8e66-4da5-abd9-75ae80369b9f", "openfda": {"upc": ["0324338510179", "0324338310106"], "unii": ["R8DG7T2D3A"], "spl_set_id": ["ac666008-a14f-43b4-9d06-ec70f45a4234"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (24338-310-10) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "24338-310-10", "marketing_start_date": "20251020"}], "brand_name": "FeraBright", "product_id": "24338-310_ac5e7507-8e66-4da5-abd9-75ae80369b9f", "dosage_form": "INJECTION", "pharm_class": ["Iron [CS]", "Parenteral Iron Replacement [EPC]"], "product_ndc": "24338-310", "generic_name": "Ferumoxytol", "labeler_name": "Azurity Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FeraBright", "active_ingredients": [{"name": "FERUMOXYTOL", "strength": "30 mg/mL"}], "application_number": "NDA219868", "marketing_category": "NDA", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}