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Molecule

Hydralazine

Also known as hydralazine hydrochloride
Available on requestCardiology
Presentations
6
Brands
0
Manufacturers
0
Available from stock
0

Hydralazine is an arteriolar vasodilator. It is available as tablets and injection for oral, intramuscular and intravenous use. MedsAcross supplies Hydralazine for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Arteriolar Vasodilator, Arteriolar Vasodilation
ATC classification
C02DB02 Hydralazine · Other blood pressure medicines, subgroup C02D, subgroup C02DB
US FDA first approval
15 January 1953
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral, Intramuscular, Intravenous
Dosage forms
Tablet, Injection
Identifiers
UNII 26NAK24LS8RxCUI 5470CAS 86-54-4DrugBank DB01275Q419987

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

Severe essential hypertension when the drug cannot be given orally or when there is an urgent need to lower blood pressure.

Source: US FDA prescribing information

How it works

of hydralazine is not fully understood, the major effects are on the cardiovascular system. Hydralazine apparently lowers blood pressure by exerting a peripheral vasodilating effect through a direct relaxation of vascular smooth muscle. Hydralazine, by altering cellular calcium metabolism, interferes with the calcium movements within the vascular smooth muscle that are responsible for initiating or maintaining the contractile state. The peripheral vasodilating effect of hydralazine results in decreased arterial blood pressure (diastolic more than systolic), decreased peripheral vascular resistance, and an increased heart rate, stroke volume and cardiac output. The preferential dilatation of arterioles, as compared to veins, minimizes postural hypotension and promotes the increase in cardiac output.

Source: US FDA prescribing information

Dosing overview

When there is urgent need, therapy in the hospitalized patient may be initiated intramuscularly or as a rapid intravenous bolus injection directly into the vein. Hydralazine Hydrochloride Injection should be used only when the drug cannot be given orally. The usual dose is 20 to 40 mg, repeated as necessary. Certain patients (especially those with marked renal damage) may require a lower dose. Blood pressure should be checked frequently. It may begin to fall within a few minutes after injection, with the average maximal decrease occurring in 10 to 80 minutes. In cases where there has been increased intracranial pressure, lowering the blood pressure may increase cerebral ischemia. Most patients can be transferred to oral hydralazine hydrochloride within 24 to 48 hours. The product should be used immediately after the vial is opened. The product should not be added to infusion solutions.

Source: US FDA prescribing information

Contraindications

Hypersensitivity to hydralazine, coronary artery disease, mitral valvular rheumatic heart disease.

Source: US FDA prescribing information

Warnings and precautions

In a few patients, hydralazine may produce a clinical picture simulating systemic lupus erythematosus including glomerulonephritis. In such patients, hydralazine should be discontinued unless the benefit-to-risk determination requires continued antihypertensive therapy with this drug. Symptoms and signs usually regress when the drug is discontinued but residua have been detected many years later. Long-term treatment with steroids may be necessary.

Source: US FDA prescribing information

Side effects

Adverse reactions with hydralazine hydrochloride are usually reversible when dosage is reduced. However, in some cases it may be necessary to discontinue the drug. The following adverse reactions have been observed, but there has not been enough systematic collection of data to support an estimate of their frequency. Common: Headache, anorexia, nausea, vomiting, diarrhea, palpitations, tachycardia, angina pectoris. Less Frequent: Digestive -constipation, paralytic ileus. Cardiovascular -hypotension, paradoxical pressor response, edema. Respiratory -dyspnea. Neurologic -peripheral neuritis, evidenced by paresthesia, numbness, and tingling, dizziness, tremors, muscle cramps, psychotic reactions characterized by depression, disorientation, or anxiety. Genitourinary -difficulty in urination.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

6 presentations of Hydralazine, sorted by availability.

MedicineManufacturerRegisterAvailability
Hydralazine 50 mg tabletOralGeneric name—US FDAAvailable on request
Hydralazine 25 mg tabletOralGeneric name—US FDAAvailable on request
Hydralazine 10 mg tabletOralGeneric name—US FDAAvailable on request
Hydralazine 100 mg tabletOralGeneric name—US FDAAvailable on request
Hydralazine 20 mg/1 mL injectionIntramuscular, intravenousGeneric name—US FDAAvailable on request
Hydralazine 400 mg/20 mL injectionIntramuscular, intravenousGeneric name—US FDAAvailable on request

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 15 January 1953Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Hydralazine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Hydralazine available for export from India?

Yes, on request. MedsAcross lists 6 presentations of Hydralazine and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Hydralazine approved by the US FDA?

Yes. The US FDA first approved Hydralazine on 15 January 1953, according to Drugs@FDA.

Does Hydralazine need cold chain shipping?

No listed presentation of Hydralazine is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Hydralazine in?

Hydralazine is classified under ATC code C02DB02 (Hydralazine).

References

  1. Hydralazine Hydrochloride prescribing information (Fresenius Kabi). U.S. National Library of Medicine, DailyMed. Retrieved 7 October 2026

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