Orange Book product · Brand (NDA)
GEODON
ZIPRASIDONE MESYLATE
Brand (NDA)NDA 020919TE APRX VIATRIS
At a glance
Jun 21, 2002
Approved
Brand (NDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 21, 2002
24 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
ZIPRASIDONE MESYLATE
Strength
EQ 20MG BASE/VIAL
Dosage form
POWDER
Route
INTRAMUSCULAR
TE code
AP
Application
NDA 020919
Product number
001
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
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.
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.
