Orange Book product · Generic (ANDA)
CEFUROXIME AXETIL
CEFUROXIME AXETIL
At a glance
Mar 29, 2006
Approved
Generic (ANDA)
Application
AB
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
CEFUROXIME AXETIL
Strength
EQ 125MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 065308
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CEFUROXIME AXETIL
- 1994CEFTINBrand (NDA)
NDA 050672 · GLAXOSMITHKLINE
- 1987CEFTINBrand (NDA)
NDA 050605 · GLAXOSMITHKLINE
- 2010CEFUROXIME AXETILGeneric (ANDA)
ANDA 065496 · ALKEM LABS LTD
- 2008CEFUROXIME AXETILGeneric (ANDA)
ANDA 065359 · ANDA REPOSITORY
- 2008CEFUROXIME AXETILGeneric (ANDA)
ANDA 065323 · SUN PHARM INDS LTD
- 2005CEFUROXIME AXETILGeneric (ANDA)
ANDA 065166 · CHARTWELL RX
- 2004CEFUROXIME AXETILGeneric (ANDA)
ANDA 065190 · ANI PHARMS
- 2003CEFUROXIME AXETILGeneric (ANDA)
ANDA 065126 · FOSUN PHARMA
- 2003CEFUROXIME AXETILGeneric (ANDA)
ANDA 065135 · LUPIN
- 2003CEFUROXIME AXETILGeneric (ANDA)
ANDA 065118 · SUN PHARM INDS LTD
- 2002CEFUROXIME AXETILGeneric (ANDA)
ANDA 065069 · APOTEX
- 2002CEFUROXIME AXETILGeneric (ANDA)
ANDA 065043 · RANBAXY LABS LTD
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.
