Wednesday, July 8, 2026

Drug profile · INN

arimoclomol citrate

arimoclomol citrate (MIPLYFFA) is a unknown. Associated with ZEVRA THERAPEUTICS, INC.. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 4
Pipeline programs 0
News articles 0
Drug details — arimoclomol citrate
US status
approved
Class
Route
ORAL
Patents
4
Programs
0
Data quality
0.89

Quick answer

arimoclomol citrate (MIPLYFFA) is a unknown. Associated with ZEVRA THERAPEUTICS, INC.. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN arimoclomol citrate
Brand MIPLYFFA
Mechanism Unknown
Route ORAL
Formulation CAPSULE

Mechanism of action

Unknown

Approval history

Authority Status Date
FDA approved
  1. US 12251445

    Gamma-hydroxybutyrate delivering compounds and processes for making and using them

    Expires Mon Mar 13 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  2. US 12076316

    Levorphanol prodrugs and processes for making and using them

    Expires Mon Aug 29 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  3. US 12012384

    Dextrorphan prodrugs and processes for making and using them

    Expires Mon Jun 13 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  4. US 11938125

    Use of Hsp70 as a regulator of enzymatic activity

    Expires Mon Mar 21 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is arimoclomol citrate?

arimoclomol citrate (MIPLYFFA) is a unknown. Associated with ZEVRA THERAPEUTICS, INC.. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for arimoclomol citrate?

MIPLYFFA is a marketed brand name for arimoclomol citrate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of arimoclomol citrate?

arimoclomol citrate 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.