Orange Book product · Brand (NDA)
CEFZIL
CEFPROZIL
At a glance
Dec 23, 1991
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 23, 1991
35 yr ago
Today
Pharmaceutical detail
Active ingredient
CEFPROZIL
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 050664
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.
- 1991CEFZILBrand (NDA)
NDA 050665 · CORDEN PHARMA
- 2024CEFPROZILGeneric (ANDA)
ANDA 090857 · ALKEM LABS LTD
- 2012CEFPROZILGeneric (ANDA)
ANDA 065351 · APOTEX INC
- 2008CEFPROZILGeneric (ANDA)
ANDA 065327 · APOTEX INC
- 2007CEFPROZILGeneric (ANDA)
ANDA 065428 · WOCKHARDT
- 2007CEFPROZILGeneric (ANDA)
ANDA 065340 · AUROBINDO PHARMA
- 2007CEFPROZILGeneric (ANDA)
ANDA 065381 · AUROBINDO PHARMA
- 2006CEFPROZILGeneric (ANDA)
ANDA 065198 · RANBAXY LABS LTD
- 2006CEFPROZILGeneric (ANDA)
ANDA 065202 · RANBAXY LABS LTD
- 2005CEFPROZILGeneric (ANDA)
ANDA 065284 · ORCHID HLTHCARE
- 2005CEFPROZILGeneric (ANDA)
ANDA 065261 · LUPIN
- 2005CEFPROZILGeneric (ANDA)
ANDA 065267 · ORCHID HLTHCARE
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.

