Orange Book product · Brand (NDA)
DESFERAL
DEFEROXAMINE MESYLATE
At a glance
May 25, 2000
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 25, 2000
26 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
DEFEROXAMINE MESYLATE
Strength
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 016267
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 2017DEFEROXAMINE MESYLATEGeneric (ANDA)
ANDA 207384 · GLAND
- 2009DEFEROXAMINE MESYLATEGeneric (ANDA)
ANDA 078718 · FRESENIUS KABI USA
- 2007DEFEROXAMINE MESYLATEGeneric (ANDA)
ANDA 078086 · HIKMA
- 2006DEFEROXAMINE MESYLATEGeneric (ANDA)
ANDA 076806 · DR REDDYS
- 2004DEFEROXAMINE MESYLATEGeneric (ANDA)
ANDA 076019 · HOSPIRA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
