Friday, July 10, 2026

Drug profile · INN

levamlodipine maleate

levamlodipine maleate (CONJUPRI) is a voltage-gated l-type calcium channel blocker. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 1
News articles 0
Drug details — levamlodipine maleate
US status
approved
Class
Route
ORAL
Patents
0
Programs
1
Data quality
0.84

Quick answer

levamlodipine maleate (CONJUPRI) is a voltage-gated l-type calcium channel blocker. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN levamlodipine maleate
Brand CONJUPRI
Mechanism Voltage-gated L-type calcium channel blocker
Target Voltage-gated L-type calcium channel
Route ORAL
Formulation TABLET

Mechanism of action

Voltage-gated L-type calcium channel blocker

Primary target: Voltage-gated L-type calcium channel

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Levamlodipine Phase 3 · Chinese Academy of · Hypertension

Related & competitor drugs

  1. amlodipine benzoate Voltage-gated L-type calcium channel blocker
  2. amlodipine besylate Voltage-gated L-type calcium channel blocker
  3. diltiazem hydrochloride Voltage-gated L-type calcium channel blocker
  4. isradipine Voltage-gated L-type calcium channel blocker
  5. nicardipine hydrochloride Voltage-gated L-type calcium channel blocker
  6. nifedipine Voltage-gated L-type calcium channel blocker

Frequently asked questions

What is levamlodipine maleate?

levamlodipine maleate (CONJUPRI) is a voltage-gated l-type calcium channel blocker. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for levamlodipine maleate?

CONJUPRI is a marketed brand name for levamlodipine maleate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of levamlodipine maleate?

levamlodipine maleate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.