Orange Book product · Brand (NDA)
GEODON
ZIPRASIDONE HYDROCHLORIDE
At a glance
Mar 29, 2006
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 29, 2006
20 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
ZIPRASIDONE HYDROCHLORIDE
Strength
EQ 10MG BASE/ML
Dosage form
SUSPENSION
Route
ORAL
TE code
Not listed
Application
NDA 021483
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 2001GEODONBrand (NDA)
NDA 020825 · VIATRIS
- 2017ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 208988 · ZYDUS LIFESCIENCES
- 2017ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 204375 · MACLEODS PHARMS LTD
- 2016ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 204117 · AUROBINDO PHARMA
- 2013ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 202395 · MYLAN
- 2012ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 090348 · CHARTWELL RX
- 2012ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 077562 · SANDOZ INC
- 2012ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 077561 · APOTEX
- 2012ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 077565 · DR REDDYS LABS INC
- 2012ZIPRASIDONE HYDROCHLORIDEGeneric (ANDA)
ANDA 077560 · LUPIN PHARMS
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.
