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enalapril tablets

Istituto Auxologico Italiano · FDA-approved active Small molecule Quality 2/100

enalapril tablets is a Small molecule drug developed by Istituto Auxologico Italiano. It is currently FDA-approved.

Enalapril tablets, marketed by Istituto Auxologico Italiano, hold a position in the cardiovascular market with a key composition patent expiring in 2028. The drug's primary strength lies in its established market presence and long-term use for primary indications, though specific details on mechanism and revenue are not provided. The primary risk is the potential increase in competition post-patent expiry in 2028.

At a glance

Generic nameenalapril tablets
SponsorIstituto Auxologico Italiano
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about enalapril tablets

What is enalapril tablets?

enalapril tablets is a Small molecule drug developed by Istituto Auxologico Italiano.

Who makes enalapril tablets?

enalapril tablets is developed and marketed by Istituto Auxologico Italiano (see full Istituto Auxologico Italiano pipeline at /company/istituto-auxologico-italiano).

What development phase is enalapril tablets in?

enalapril tablets is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing