Orange Book product · Brand (NDA)
PERTOFRANE
DESIPRAMINE HYDROCHLORIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
DESIPRAMINE HYDROCHLORIDE
Strength
50MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
NDA 013621
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1982NORPRAMINBrand (NDA)
NDA 014399 · VALIDUS PHARMS
- 2021DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209785 · ALEMBIC
- 2017DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 204963 · INGENUS PHARMS LLC
- 2016DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 205153 · ANI PHARMS
- 2016DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 207433 · HERITAGE
- 2016DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 208105 · AMNEAL PHARMS CO
- 1996DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074430 · ACTAVIS TOTOWA
- 1988DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072103 · CHARTWELL RX
- 1987DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071803 · ANI PHARMS
- 1987DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071602 · ACTAVIS TOTOWA
- 1987DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071766 · ACTAVIS TOTOWA
- 1987DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071864 · USL PHARMA
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.
