MedPath

Diltiazem

Generic Name
Diltiazem
Brand Names
Cardizem, Cartia, Matzim, Taztia, Tiadylt, Tiazac
Drug Type
Small Molecule
Chemical Formula
C22H26N2O4S
CAS Number
42399-41-7
Unique Ingredient Identifier
EE92BBP03H

Overview

Diltiazem is a benzothiazepine derivative with antihypertensive and vasodilating properties. Approved in 1982 by the FDA, it is a member of the non-dihydropyridine calcium channel blockers drug class. It works through various mechanisms of action, but it primarily works by inhibiting the calcium influx into cardiac and vascular smooth muscle during depolarization. Compared to dihydropyridine drugs, such as nifedipine, that preferentially act on vascular smooth muscle and verapamil that directly acts on the heart muscle, diltiazem displays an intermediate specificity to target both the cardiac and vascular smooth muscle. Being a potent vasodilator, diltiazem is used clinically as an antihypertensive, anti-arrhythmic, and as an anti-anginal agent for the management of cardiovascular conditions such as hypertension, chronic stable angina, atrial fibrillation, atrial flutter. Apart from its main FDA-approved indications, diltiazem has also been used for numerous off-label indications, such as anal fissures (in topical formulations), migraine prophylaxis, pulmonary hypertension, and rest-related cramps in the lower extremities. Typically available in extended-release oral and intravenous formulations, diltiazem is marketed under various brand names with Cardizem and Tiazac being the most common ones.

Indication

Oral Indicated for the management of hypertension, to lower blood pressure, alone or in combination with other antihypertensive agents. Indicated for use to improve exercise tolerance in patients with chronic stable angina. Indicated for the management of variant angina (Prinzmetal's angina). Intravenous Indicated for the short-term management of atrial fibrillation or atrial flutter for temporary control of rapid ventricular rate. Indicated for the rapid conversion of paroxysmal supraventricular tachycardias (PSVT) to sinus rhythm. This includes AV nodal reentrant tachycardias and reciprocating tachycardias associated with an extranodal accessory pathway such as the WPW syndrome or short PR syndrome. Off-label Indicated for off-label uses in anal fissures (as topical formulation), migraine prophylaxis, cramps in lower leg related to rest, pulmonary hypertension, idiopathic dilated cardiomyopathy, and proteinuria associated with diabetic nephropathy.

Associated Conditions

  • Angina Pectoris, Variant
  • Anginal Pain
  • Atrial Fibrillation
  • Atrial Flutter
  • Chronic Stable Angina Pectoris
  • Dilated Cardiomyopathies, Idiopathic
  • Fissure;Anal
  • Hypertension
  • Paroxysmal Supraventricular Tachycardia (PSVT)
  • Proteinuria
  • Pulmonary Hypertension (PH)
  • Leg cramps
  • Prophylaxis of migraine headaches

Research Report

Published: Aug 6, 2025

Diltiazem (DB00343): A Comprehensive Pharmacological and Clinical Monograph

Section I: Executive Summary

Diltiazem is a non-dihydropyridine calcium channel blocker of the benzothiazepine class, distinguished by its balanced effects on both cardiac tissue and vascular smooth muscle. Its primary mechanism of action involves the inhibition of L-type calcium channels, which results in a constellation of therapeutic effects, including negative chronotropy (reduced heart rate), dromotropy (slowed atrioventricular conduction), and mild negative inotropy (reduced cardiac contractility), coupled with potent coronary and peripheral vasodilation.

Clinically, diltiazem is well-established for the management of hypertension, chronic stable angina, and variant (Prinzmetal's) angina. In its intravenous formulation, it is a cornerstone for the acute management of supraventricular arrhythmias, particularly for rate control in atrial fibrillation or flutter and for the conversion of paroxysmal supraventricular tachycardia. Its therapeutic scope has expanded to include numerous off-label applications, such as the topical treatment of anal fissures, and it is the subject of significant investigational research for disease modification in preclinical hypertrophic cardiomyopathy, treatment of coronary microvascular dysfunction, and even as a potential anticancer agent through a newly discovered mechanism involving urokinase receptor (uPAR) inhibition.

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/08/05
Not Applicable
Not yet recruiting
Second Affiliated Hospital, School of Medicine, Zhejiang University
2025/05/28
Phase 4
Recruiting
Anne E. Zepeski
2025/02/11
Phase 1
Active, not recruiting
2024/11/25
Phase 1
Completed
2024/11/18
Phase 1
Completed
2024/10/28
Phase 1
Completed
2024/08/15
Phase 1
Completed
2024/08/02
Phase 4
Completed
2024/02/23
Phase 3
Not yet recruiting
Oman Medical Speciality Board
2022/10/03
Phase 2
Withdrawn

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Oceanside Pharmaceuticals
68682-521
ORAL
360 mg in 1 1
4/1/2020
TWi Pharmaceuticals, Inc.
24979-183
ORAL
120 mg in 1 1
12/1/2023
Upsher-Smith Laboratories, LLC
24979-183
ORAL
120 mg in 1 1
12/1/2023
NuCare Pharmaceuticals,Inc.
68071-4664
ORAL
120 mg in 1 1
2/17/2021
GLENMARK PHARMACEUTICALS INC., USA
68462-851
ORAL
90 mg in 1 1
3/23/2021
NuCare Pharmaceuticals,Inc.
68071-4371
ORAL
120 mg in 1 1
2/16/2021
Actavis Pharma, Inc.
62037-698
ORAL
240 mg in 1 1
7/25/2022
Aidarex Pharmaceuticals LLC
33261-183
ORAL
60 mg in 1 1
12/29/2013
Cipla USA, Inc.
69097-993
ORAL
180 mg in 1 1
5/1/2023
PuraCap Laboratories LLC
24658-346
ORAL
420 mg in 1 1
1/8/2019

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
HERBESSER R100 CAP 100MG (JAPAN)
N/A
N/A
N/A
9/30/2003

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
MED DILTIAZEM - TAB 60MG
medican pharma incorporated
02189046
Tablet - Oral
60 MG
3/12/1997
DILTIAZEM HYDROCHLORIDE INJECTION
02244728
Solution - Intravenous
5 MG / ML
1/9/2002
DILTIAZEM-CD
PRO DOC LIMITEE
02231472
Capsule (Extended Release) - Oral
120 MG
6/1/1998
DILTIAZEM-60 TAB 60MG
PRO DOC LIMITEE
00828777
Tablet - Oral
60 MG
12/31/1989
CARDIZEM
biovail pharmaceuticals canada division of biovail corporation
02097370
Tablet - Oral
30 MG
12/31/1995
CARDIZEM
biovail pharmaceuticals canada division of biovail corporation
02097389
Tablet - Oral
60 MG
12/31/1995
CARDIZEM CD
bausch health, canada inc.
02097265
Capsule (Extended Release) - Oral
240 MG
12/31/1995
CARDIZEM CD
bausch health, canada inc.
02097249
Capsule (Extended Release) - Oral
120 MG
12/31/1995
MAR-DILTIAZEM CD
marcan pharmaceuticals inc
02484072
Capsule (Controlled-Delivery) - Oral
180 MG
3/30/2020
TEVA-DILTIAZEM HCL ER
bausch health, canada inc.
02271605
Capsule (Extended Release) - Oral
120 MG
1/30/2006

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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