Orange Book product · Generic (ANDA)
ENALAPRILAT
ENALAPRILAT
At a glance
Aug 22, 2000
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 22, 2000
26 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
ENALAPRILAT
Strength
1.25MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 075571
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ENALAPRILAT
- 1988VASOTECBrand (NDA)
NDA 019309 · BIOVAIL LABS INTL
- 2008ENALAPRILATGeneric (ANDA)
ANDA 078687 · HIKMA FARMACEUTICA
- 2000ENALAPRILATGeneric (ANDA)
ANDA 075634 · CHARTWELL INJECTABLE
- 2000ENALAPRILATGeneric (ANDA)
ANDA 075578 · DR REDDYS
- 2000ENALAPRILATGeneric (ANDA)
ANDA 075456 · HOSPIRA
- 2000ENALAPRILATGeneric (ANDA)
ANDA 075458 · HOSPIRA
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.
