DILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE
Details
- Status
- Prescription
- First Approved
- 2025-02-21
- Routes
- INTRAVENOUS
- Dosage Forms
- SOLUTION
DILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE Approval History
What DILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE Treats
3 indicationsDILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE is approved for 3 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Hypertension
- Angina
- Coronary Artery Spasm
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Active Pipeline
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Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
DILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE FDA Label Details
ProIndications & Usage
FDA Label (PDF)Diltiazem hydrochloride extended-release capsules are indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medications. Diltiazem hydrochloride extended-release capsules are indicated for the management of chronic stable angina and angina due to coronary artery spasm.
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.