Orange Book product · Generic (ANDA)
AMOXICILLIN
AMOXICILLIN
At a glance
Dec 28, 2006
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 28, 2006
19 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
AMOXICILLIN
Strength
200MG/5ML
Dosage form
FOR SUSPENSION
Route
ORAL
TE code
AB
Application
ANDA 065334
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of AMOXICILLIN
- 1999AMOXILBrand (NDA)
NDA 050760 · US ANTIBIOTICS
- —AMOXILBrand (NDA)
NDA 050459 · GLAXOSMITHKLINE
- —AMOXILBrand (NDA)
NDA 050460 · GLAXOSMITHKLINE
- 2022AMOXICILLINGeneric (ANDA)
ANDA 207471 · MICRO LABS
- 2014AMOXICILLINGeneric (ANDA)
ANDA 204030 · AUROBINDO PHARMA LTD
- 2007AMOXICILLINGeneric (ANDA)
ANDA 065319 · CHARTWELL RX
- 2007AMOXICILLINGeneric (ANDA)
ANDA 065387 · SANDOZ
- 2007AMOXICILLINGeneric (ANDA)
ANDA 065378 · SANDOZ
- 2007AMOXICILLINGeneric (ANDA)
ANDA 065291 · HIKMA PHARMS
- 2006AMOXICILLINGeneric (ANDA)
ANDA 065322 · HIKMA
- 2006AMOXICILLINGeneric (ANDA)
ANDA 065325 · HIKMA
- 2005AMOXICILLINGeneric (ANDA)
ANDA 065271 · AUROBINDO
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.
