Saturday, July 11, 2026

Drug profile · INN

dimenhydrinate

dimenhydrinate (DIMENHYDRINATE) is a histamine h1 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 1
News articles 0
Drug details — dimenhydrinate
US status
approved
Class
Route
INJECTION
Patents
0
Programs
1
Data quality
0.89

Quick answer

dimenhydrinate (DIMENHYDRINATE) is a histamine h1 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN dimenhydrinate
Brand DIMENHYDRINATE
Mechanism Histamine H1 receptor antagonist
Target Histamine H1 receptor
Route INJECTION
Formulation LIQUID

Mechanism of action

Histamine H1 receptor antagonist

Primary target: Histamine H1 receptor

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. CHE24001 Phase 1 · Anaxis Pharma · No therapeutic indication in the current trial with healthy

Related & competitor drugs

  1. azelastine hydrochloride Histamine H1 receptor antagonist
  2. brompheniramine maleate Histamine H1 receptor antagonist
  3. carbinoxamine maleate Histamine H1 receptor antagonist
  4. cetirizine hydrochloride Histamine H1 receptor antagonist
  5. chlorpheniramine maleate Histamine H1 receptor antagonist
  6. clemastine fumarate Histamine H1 receptor antagonist

Frequently asked questions

What is dimenhydrinate?

dimenhydrinate (DIMENHYDRINATE) is a histamine h1 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for dimenhydrinate?

DIMENHYDRINATE is a marketed brand name for dimenhydrinate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of dimenhydrinate?

dimenhydrinate 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.