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Data updated: May 26, 2026

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE (nicardipine hydrochloride)

Cardiovascular Approved 2008-07-24

Nicardipine hydrochloride helps patients with high blood pressure and chronic stable angina, a condition involving chest pain during physical exertion. It is used as a standalone therapy or in combination with other medications, such as beta-blockers, to manage these cardiovascular conditions. When used to lower blood pressure, it is important to monitor the drug's effect throughout the dosing cycle due to potential differences in its impact between peak and trough levels.

Source: FDA Label • Cipla

How NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE Works

This medication works by blocking the movement of calcium ions into cardiac and vascular smooth muscle cells through specific channels. By preventing this influx, the drug helps relax the smooth muscle in blood vessels, particularly those in the heart, with minimal impact on the heart's contraction strength. This selective relaxation of the vascular system helps improve blood flow and manage pressure.

3
Indications
--
Phase 3 Trials
17
Years on Market

Details

Status
Prescription
First Approved
2008-07-24
Routes
INTRAVENOUS
Dosage Forms
INJECTABLE

Companies

Active Ingredient: NICARDIPINE HYDROCHLORIDE

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE Approval History

2009
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2013
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2020
2021
2022
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2024
2025
2026
Original
New Indication
New Form
Label Update
26 FDA actions from 2008 to 2025
Oct 2025 ORIGINAL
Update
Jun 2025 SUPPL
Mfg · Manufacturing (CMC)
Mar 2025 SUPPL
Label · Labeling

What NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE Treats

2 indications

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE is approved for 2 conditions since its original approval in 2008. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Angina
  • Hypertension
Source: FDA Label

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE Competitive Set

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Clinical Trial Registry

2 trials
Trial Sponsor ID Phase Status Title
NCT03098680 PRIME PRIME (A094136) Ph 1 terminated A Study of the Pharmacokinetic and Pharmacodynamic Responses in Healthy and Altered Human Cardiovascular Systems
NCT01810302 results posted 034-2013 Ph 2 terminated Safety Study of Nicardipine to Treat Cerebral Vasospasm
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Active Pipeline

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Key Completed Trials

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Trial Timeline

Full development history with FDA approval milestones

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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.

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE FDA Label Details

Indications & Usage

FDA Label (PDF)

NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE is indicated for the treatment of Angina; Hypertension.

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.