Orange Book product · Generic (ANDA)
DESLORATADINE
DESLORATADINE
At a glance
Jul 12, 2010
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 12, 2010
16 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
DESLORATADINE
Strength
2.5MG
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
TE code
Not listed
Application
ANDA 078367
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DESLORATADINE
- 2005CLARINEXBrand (NDA)
NDA 021312 · ORGANON
- 2004CLARINEXBrand (NDA)
NDA 021300 · ORGANON LLC
- 2001CLARINEXBrand (NDA)
NDA 021165 · ORGANON
- 2016DESLORATADINEGeneric (ANDA)
ANDA 202936 · TARO
- 2015DESLORATADINEGeneric (ANDA)
ANDA 202592 · TARO
- 2012DESLORATADINEGeneric (ANDA)
ANDA 078355 · AJENAT PHARMS
- 2012DESLORATADINEGeneric (ANDA)
ANDA 078351 · NATCO PHARMA USA
- 2011DESLORATADINEGeneric (ANDA)
ANDA 078361 · PERRIGO
- 2011DESLORATADINEGeneric (ANDA)
ANDA 078365 · DR REDDYS LABS LTD
- 2010DESLORATADINEGeneric (ANDA)
ANDA 078364 · CHARTWELL RX
- 2010DESLORATADINEGeneric (ANDA)
ANDA 078359 · SUN PHARM INDS
- 2010DESLORATADINEGeneric (ANDA)
ANDA 078352 · LUPIN PHARMS
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.
