Orange Book product · Generic (ANDA)
FOSINOPRIL SODIUM
FOSINOPRIL SODIUM
At a glance
Apr 20, 2005
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 20, 2005
21 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
FOSINOPRIL SODIUM
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 077222
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FOSINOPRIL SODIUM
- 1991MONOPRILBrand (NDA)
NDA 019915 · BRISTOL MYERS SQUIBB
- 2016FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 205670 · PRINSTON INC
- 2011FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 091163 · AUROBINDO PHARMA LTD
- 2006FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 077531 · WATSON LABS
- 2005FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076906 · APOTEX
- 2004FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076987 · WATSON LABS
- 2004FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076620 · ACTAVIS LABS FL INC
- 2004FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076188 · UPSHER SMITH LABS
- 2004FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076483 · CHARTWELL RX
- 2004FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076580 · RANBAXY LABS LTD
- 2003FOSINOPRIL SODIUMGeneric (ANDA)
ANDA 076139 · TEVA
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.
