Enalapril Maleate
ENALAPRIL MALEATE TABLETS, USP
Approved
Approval ID
d59a23ba-9e28-42a3-8bfe-a3742fdfdebe
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 1, 2011
Manufacturers
FDA
Med Health Pharma, LLC
DUNS: 962603812
Products 4
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Enalapril Maleate
PRODUCT DETAILS
NDC Product Code51138-036
Application NumberANDA075483
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 1, 2011
Generic NameEnalapril Maleate
INGREDIENTS (1)
Enalapril MaleateActive
Quantity: 20 mg in 1 1
Code: 9O25354EPJ
Classification: ACTIB
Enalapril Maleate
PRODUCT DETAILS
NDC Product Code51138-033
Application NumberANDA075483
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 1, 2011
Generic NameEnalapril Maleate
INGREDIENTS (1)
Enalapril MaleateActive
Quantity: 2.5 mg in 1 1
Code: 9O25354EPJ
Classification: ACTIB
Enalapril Maleate
PRODUCT DETAILS
NDC Product Code51138-034
Application NumberANDA075483
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 1, 2011
Generic NameEnalapril Maleate
INGREDIENTS (1)
Enalapril MaleateActive
Quantity: 5 mg in 1 1
Code: 9O25354EPJ
Classification: ACTIB
Enalapril Maleate
PRODUCT DETAILS
NDC Product Code51138-035
Application NumberANDA075483
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 1, 2011
Generic NameEnalapril Maleate
INGREDIENTS (1)
Enalapril MaleateActive
Quantity: 10 mg in 1 1
Code: 9O25354EPJ
Classification: ACTIB