Enalapril Maleate

Product NDC

70518-1339

11-digit product format

705181339

Labeler code

70518

Product ID

70518-1339_92446883-5ba5-81b9-e053-2995a90a1c46

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Enalapril Maleate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075657

Marketing category

ANDA

Marketing start

2018-08-02

Marketing end

0000-00-00

Substance

ENALAPRIL MALEATE

Active strength

3 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record