desferal
Generic: deferoxamine mesylate
Labeler: novartis pharmaceuticals corporationDrug Facts
Product Profile
Brand Name
desferal
Generic Name
deferoxamine mesylate
Labeler
novartis pharmaceuticals corporation
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
deferoxamine mesylate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0078-0467
Product ID
0078-0467_9f58db85-c282-46eb-94ba-594e2092ddf2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA016267
Listing Expiration
2026-12-31
Marketing Start
1968-04-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00780467
Hyphenated Format
0078-0467
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
desferal (source: ndc)
Generic Name
deferoxamine mesylate (source: ndc)
Application Number
NDA016267 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 4 VIAL in 1 CARTON (0078-0467-91) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0078-0467-61)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "9f58db85-c282-46eb-94ba-594e2092ddf2", "openfda": {"unii": ["V9TKO7EO6K"], "rxcui": ["1731350", "1731352"], "spl_set_id": ["a7174843-5965-49fc-b842-f7eff7b48bbc"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (0078-0467-91) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0078-0467-61)", "package_ndc": "0078-0467-91", "marketing_start_date": "19680402"}], "brand_name": "Desferal", "product_id": "0078-0467_9f58db85-c282-46eb-94ba-594e2092ddf2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "0078-0467", "generic_name": "deferoxamine mesylate", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desferal", "active_ingredients": [{"name": "DEFEROXAMINE MESYLATE", "strength": "500 mg/1"}], "application_number": "NDA016267", "marketing_category": "NDA", "marketing_start_date": "19680402", "listing_expiration_date": "20261231"}