Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 016267

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DESFERAL (DEFEROXAMINE MESYLATE)
500MG/VIAL
Marketing Status: Prescription

Active Ingredient: DEFEROXAMINE MESYLATE
Proprietary Name: DESFERAL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N016267
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

DESFERAL (DEFEROXAMINE MESYLATE)
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued

Active Ingredient: DEFEROXAMINE MESYLATE
Proprietary Name: DESFERAL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N016267
Product Number: 002
Approval Date: May 25, 2000
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information