ENALAPRILAT (Hospira, Inc.)


Welcome to the PulseAid listing for the ENALAPRILAT drug offered from Hospira, Inc.. This Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Hospira, Inc.
NON-PROPRIETARY NAME: ENALAPRILAT
SUBSTANCE NAME: ENALAPRILAT
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2005-08-24
END MARKETING DATE: 0000-00-00


ENALAPRILAT HUMAN PRESCRIPTION DRUG Details:

Item DescriptionENALAPRILAT from Hospira, Inc.
LABELER NAME: Hospira, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1.25(mg/mL)
START MARKETING DATE: 2005-08-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0409-2122_e6dc115e-1410-428b-8b85-e96d191f2f71
PRODUCT NDC: 0409-2122
APPLICATION NUMBER: ANDA075458

Other ENALAPRILAT Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Cardinal HealthEnalaprilat
Hospira, Inc.ENALAPRILAT
Teva Parenteral Medicines, Inc.Enalaprilat
West-ward Pharmaceutical CorpEnalaprilat