Orange Book product · Generic (ANDA)
ESCITALOPRAM OXALATE
ESCITALOPRAM OXALATE
At a glance
Sep 12, 2012
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 12, 2012
14 yr ago
Today
Pharmaceutical detail
Active ingredient
ESCITALOPRAM OXALATE
Strength
EQ 5MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 202280
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ESCITALOPRAM OXALATE
- 2025ESCITALOPRAMBrand (NDA)
NDA 219130 · ALMATICA
- 2002LEXAPROBrand (NDA)
NDA 021365 · ABBVIE
- 2002LEXAPROBrand (NDA)
NDA 021323 · ABBVIE
- 2026ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 091655 · MICRO LABS
- 2025ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 215177 · ASCENT PHARMS INC
- 2017ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 205619 · AMNEAL PHARMS
- 2016ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 202754 · MACLEODS PHARMS LTD
- 2015ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 078032 · PRINSTON INC
- 2015ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 203967 · ANTRIM PHARMS LLC
- 2015ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 077550 · NOVITIUM PHARMA
- 2013ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 090477 · CHARTWELL MOLECULAR
- 2012ESCITALOPRAM OXALATEGeneric (ANDA)
ANDA 077512 · AIPING PHARM INC
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.

