Orange Book product · Generic (ANDA)
DESLORATADINE
DESLORATADINE
At a glance
May 26, 2016
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 26, 2016
10 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
DESLORATADINE
Strength
0.5MG/ML
Dosage form
SOLUTION
Route
ORAL
TE code
Not listed
Application
ANDA 202936
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
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
- 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
- 2010DESLORATADINEGeneric (ANDA)
ANDA 078367 · REDDYS
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.
