Orange Book product · Brand (NDA)
SERZONE
NEFAZODONE HYDROCHLORIDE
At a glance
Dec 22, 1994
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 22, 1994
31 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
NEFAZODONE HYDROCHLORIDE
Strength
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 020152
Product number
001
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.
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076072 · ANI PHARMS
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076129 · AUROBINDO PHARMA USA
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076302 · CHARTWELL RX
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076309 · DR REDDYS LABS INC
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 075763 · IVAX SUB TEVA PHARMS
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076196 · ROXANE
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076409 · SUN PHARM INDS LTD
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076037 · TEVA
- 2003NEFAZODONE HYDROCHLORIDEGeneric (ANDA)
ANDA 076073 · WATSON LABS
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.

