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Drug profile · INN

hydrocortisone

HYDROCORTISONE AGUETTANT

approved H02AB09
US status
approved
Patents linked
5
News articles
0

Quick answer

hydrocortisone (HYDROCORTISONE AGUETTANT) is an FDA-listed pharmaceutical active ingredient. Associated with Takeda Pharmaceuticals International AG. Route of administration: for rx compounding. Current US regulatory status: approved.

Key facts

INN hydrocortisone
Brand HYDROCORTISONE AGUETTANT
Route FOR RX COMPOUNDING
Formulation POWDER
ATC code H02AB09
Originator Takeda Pharmaceuticals International AG

Related patents

Search patents →

  1. US 12419831

    Hydrocortisone oral liquid formulations

    Expires Mon Sep 18 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  2. US 12133914

    Hydrocortisone oral liquid formulations

    Expires Mon Oct 31 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  3. US 11904046

    Hydrocortisone oral liquid formulations

    Expires Mon Feb 15 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  4. US 6803359

    Inhibition of abnormal cell growth with corticotropin-releasing hormone analogs

    Expires Mon Oct 07 2024 00:00:00 GMT+0000 (Coordinated Universal Time)

    expired

  5. US 6319900

    Inhibition of abnormal cell growth with corticotropin-releasing hormone analogs

    Expires Mon Nov 15 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

    expired

Frequently asked questions

What is hydrocortisone?

hydrocortisone (HYDROCORTISONE AGUETTANT) is an FDA-listed pharmaceutical active ingredient. Associated with Takeda Pharmaceuticals International AG. Route of administration: for rx compounding. Current US regulatory status: approved.

What is the brand name for hydrocortisone?

HYDROCORTISONE AGUETTANT is a marketed brand name for hydrocortisone. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of hydrocortisone?

hydrocortisone 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.