Orange Book product · Generic (ANDA)
ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
At a glance
Sep 18, 2001
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 18, 2001
25 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
Strength
5MG;12.5MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 075788
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
- 1995VASERETICBrand (NDA)
NDA 019221 · BAUSCH
- 2004ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076486 · MPP PHARMA
- 2003ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075736 · IVAX SUB TEVA PHARMS
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075909 · SENORES PHARMS
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 076116 · CHARTWELL RX
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075727 · COSETTE
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075624 · RISING
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.
