Orange Book product · Generic (ANDA)
IMIPRAMINE HYDROCHLORIDE
IMIPRAMINE HYDROCHLORIDE
At a glance
May 22, 1984
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 22, 1984
42 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
IMIPRAMINE HYDROCHLORIDE
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 087846
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of IMIPRAMINE HYDROCHLORIDE
- —TOFRANILBrand (NDA)
NDA 011838 · NOVARTIS
- —JANIMINEBrand (NDA)
NDA 017895 · ABBOTT
- —PRESAMINEBrand (NDA)
NDA 011836 · SANOFI AVENTIS US
- 2012IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040903 · LEADING
- 2010IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 090441 · CHARTWELL
- 2008IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040751 · OXFORD PHARMS
- 1990IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 081048 · SUN PHARM INDUSTRIES
- 1990IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 081049 · SUN PHARM INDUSTRIES
- 1990IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 081050 · SUN PHARM INDUSTRIES
- 1987IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089422 · PAR PHARM
- 1987IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089497 · PAR PHARM
- 1983IMIPRAMINE HYDROCHLORIDEGeneric (ANDA)
ANDA 088292 · STRIDES PHARMA INTL
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.
