Orange Book product · Generic (ANDA)
DESIPRAMINE HYDROCHLORIDE
DESIPRAMINE HYDROCHLORIDE
At a glance
Dec 26, 2017
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 26, 2017
8 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
DESIPRAMINE HYDROCHLORIDE
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 204963
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DESIPRAMINE HYDROCHLORIDE
- 1982NORPRAMINBrand (NDA)
NDA 014399 · VALIDUS PHARMS
- —PERTOFRANEBrand (NDA)
NDA 013621 · SANOFI AVENTIS US
- 2021DESIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209785 · ALEMBIC
- 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.
