Orange Book product · Generic (ANDA)
FEXOFENADINE HYDROCHLORIDE
FEXOFENADINE HYDROCHLORIDE
At a glance
Jul 25, 2012
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 25, 2012
14 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
FEXOFENADINE HYDROCHLORIDE
Strength
30MG/5ML
Dosage form
SUSPENSION
Route
ORAL
TE code
Not listed
Application
ANDA 201311
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FEXOFENADINE HYDROCHLORIDE
- 2011CHILDREN'S ALLEGRA ALLERGYBrand (NDA)
NDA 201373 · CHATTEM SANOFI
- 2011CHILDREN'S ALLEGRA ALLERGYBrand (NDA)
NDA 021909 · CHATTEM SANOFI
- 2011ALLEGRA ALLERGYBrand (NDA)
NDA 020872 · CHATTEM SANOFI
- 2006ALLEGRABrand (NDA)
NDA 021963 · CHATTEM SANOFI
- 1996ALLEGRABrand (NDA)
NDA 020625 · CHATTEM SANOFI
- 2025FEXOFENADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 219032 · CONTRACT PHARMACAL
- 2023FEXOFENADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 213466 · AUROBINDO PHARMA LTD
- 2020FEXOFENADINE HYDROCHLORIDEGeneric (ANDA)
ANDA 212971 · L PERRIGO CO
- 2019FEXOFENADINE HYDROCHLORIDE ALLERGYGeneric (ANDA)
ANDA 211075 · GRANULES
- 2018FEXOFENADINE HYDROCHLORIDE ALLERGYGeneric (ANDA)
ANDA 210137 · UNIQUE
- 2017CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGYGeneric (ANDA)
ANDA 208123 · TARO
- 2016CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGYGeneric (ANDA)
ANDA 204097 · HETERO LABS LTD V
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.
