deferoxamine mesylate

Generic: deferoxamine mesylate

Labeler: gland pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deferoxamine mesylate
Generic Name deferoxamine mesylate
Labeler gland pharma limited
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

deferoxamine mesylate 500 mg/1

Manufacturer
Gland Pharma Limited

Identifiers & Regulatory

Product NDC 68083-172
Product ID 68083-172_316b7751-fbd4-4b19-b7b7-701554fd3b21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207384
Listing Expiration 2026-12-31
Marketing Start 2017-10-09

Pharmacologic Class

Classes
iron chelating activity [moa] iron chelator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68083172
Hyphenated Format 68083-172

Supplemental Identifiers

RxCUI
1731345 1731350
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 deferoxamine mesylate (source: ndc)
Generic Name deferoxamine mesylate (source: ndc)
Application Number ANDA207384 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 4 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68083-172-01)
source: ndc

Packages (1)

68083-172-01 4 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68083-172-01)

Ingredients (1)

deferoxamine mesylate (500 mg/1)

Linked Drug Pages (1)

Deferoxamine mesylate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "316b7751-fbd4-4b19-b7b7-701554fd3b21", "openfda": {"unii": ["V9TKO7EO6K"], "rxcui": ["1731345", "1731350"], "spl_set_id": ["598fba68-f46e-4b6e-894c-63c2940b2063"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68083-172-01)", "package_ndc": "68083-172-01", "marketing_start_date": "20171009"}], "brand_name": "Deferoxamine mesylate", "product_id": "68083-172_316b7751-fbd4-4b19-b7b7-701554fd3b21", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "68083-172", "generic_name": "Deferoxamine mesylate", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferoxamine mesylate", "active_ingredients": [{"name": "DEFEROXAMINE MESYLATE", "strength": "500 mg/1"}], "application_number": "ANDA207384", "marketing_category": "ANDA", "marketing_start_date": "20171009", "listing_expiration_date": "20261231"}