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
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.
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
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
HERBESSER FOR INJECTION 50 mg/ampoule | SIN06012P | INJECTION, POWDER, FOR SOLUTION | 50 mg/ampoule | 6/5/1991 | |
HERBESSER 90 SR CAPSULE 90 mg | SIN06791P | CAPSULE | 90 mg | 12/20/1991 | |
HERBESSER 60 TABLET 60 mg | SIN00430P | TABLET | 60 mg | 4/28/1988 | |
HERBESSER R200 CAPSULES 200 mg | SIN10061P | CAPSULE | 200mg | 9/29/1998 | |
HERBESSER TABLET 30 mg | SIN00428P | TABLET | 30 mg | 4/28/1988 | |
HERBESSER R100 CAPSULES 100 mg | SIN10062P | CAPSULE | 100 mg | 9/29/1998 | |
HERBESSER FOR INJECTION 10 mg/ampoule | SIN06013P | INJECTION, POWDER, FOR SOLUTION | 10 mg/ampoule | 6/5/1991 |
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 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
APO-DILTIAZEM CD diltiazem hydrochloride 240mg capsule bottle | 90922 | Medicine | A | 9/17/2002 | |
DILTIAZEM SANDOZ CD diltiazem hydrochloride 240mg capsule bottle | 131300 | Medicine | A | 2/26/2007 | |
DANZEM diltiazem hydrochloride 60mg tablet bottle | 184086 | Medicine | A | 7/20/2012 | |
APO-DILTIAZEM CD diltiazem hydrochloride 180mg capsules blisterpack | 80555 | Medicine | A | 5/27/2002 | |
DILTIAZEM SANDOZ CD diltiazem hydrochloride 360mg capsule bottle (unprinted) | 131304 | Medicine | A | 2/26/2007 | |
CARDIZEM CD 180mg capsule blister pack | 46818 | Medicine | A | 11/10/1993 | |
APO-DILTIAZEM CD diltiazem hydrochloride 240mg capsules blisterpack | 80553 | Medicine | A | 5/27/2002 | |
Diltiazem hydrochloride ER Capsules 60mg | 396805 | Medicine | A | 9/30/2022 | |
VASOCARDOL diltiazem hydrochloride 60mg tablet bottle | 73180 | Medicine | A | 5/9/2000 | |
DILTIAZEM SANDOZ CD diltiazem hydrochloride 180mg capsule bottle | 131298 | Medicine | A | 2/26/2007 |
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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