Enalaprilat

Product NDC

0703-8401

11-digit product format

007038401

Labeler code

0703

Product ID

0703-8401_d8d25b72-f417-43f6-9966-05a6439db304

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Enalaprilat

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA075578

Marketing category

ANDA

Marketing start

2005-10-06

Marketing end

0000-00-00

Substance

ENALAPRILAT

Active strength

1 mg/mL

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record