Orange Book product · Generic (ANDA)
ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
At a glance
Oct 15, 2001
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 15, 2001
25 yr ago
Today
Pharmaceutical detail
Active ingredient
ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
Strength
5MG;12.5MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 075909
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 076116 · CHARTWELL RX
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075727 · COSETTE
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075624 · RISING
- 2001ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 075788 · TARO PHARM INDS
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.
