desferal

Generic: deferoxamine mesylate

Labeler: novartis pharmaceuticals corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name desferal
Generic Name deferoxamine mesylate
Labeler novartis pharmaceuticals corporation
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

deferoxamine mesylate 500 mg/1

Manufacturer
Novartis Pharmaceuticals Corporation

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
iron chelating activity [moa] iron chelator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00780467
Hyphenated Format 0078-0467

Supplemental Identifiers

RxCUI
1731350 1731352
UNII
V9TKO7EO6K

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 4 VIAL in 1 CARTON (0078-0467-91) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0078-0467-61)
source: ndc

Packages (1)

Ingredients (1)

deferoxamine mesylate (500 mg/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"}