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Molecule

Phentolamine

Also known as phentolamine mesylate
Available on requestCold chainCardiologyAntidotes
Presentations
4
Brands
2
Manufacturers
2
Available from stock
0

Phentolamine is an alpha-adrenergic blocker indicated for adult and pediatric patients ages 3 years and older for the reversal of soft-tissue anesthesia, i.e., among other approved uses. MedsAcross supplies Phentolamine 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
Alpha-Adrenergic Blocker, Adrenergic alpha-Antagonists
ATC classification
C04AB01 Phentolamine · Peripheral vasodilators, subgroup C04A, subgroup C04ABV03AB36 Phentolamine · Antidote
US FDA first approval
30 January 1952
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intramuscular, Intravenous, Ophthalmic, Submucosal
Dosage forms
Injection, Eye drops, Powder for injection
Identifiers
UNII Z468598HBVRxCUI 8153CAS 50-60-2DrugBank DB00692Q420360

Clinical information

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

Uses

1. INDICATONS AND USAGE OraVerse an alpha adrenergic blocker, is indicated for adult and pediatric patients ages 3 years and older for the reversal of soft-tissue anesthesia, i.e., anesthesia of the lip and tongue, and the associated functional deficits resulting from an intraoral submucosal injection of a local anesthetic containing a vasoconstrictor. OraVerse, an alpha adrenergic blocker, is indicated for adult and pediatric patients ages 3 years and older for the reversal of soft-tissue anesthesia, i.e., anesthesia of the lip and tongue, and the associated functional deficits resulting from an intraoral submucosal injection of a local anesthetic containing a vasoconstrictor.

Source: US FDA prescribing information

How it works

The mechanism by which OraVerse accelerates reversal of soft-tissue anesthesia and the associated functional deficits is not fully understood. Phentolamine mesylate, the active ingredient in OraVerse, produces an alpha-adrenergic block of relatively short duration resulting in vasodilatation when applied to vascular smooth muscle. In an animal model, OraVerse increased local blood flow in submucosal tissue of the dog when given after an intraoral injection of lidocaine 2% with 1:100,000 epinephrine.

Source: US FDA prescribing information

Dosing overview

2. DOSAGE AND ADMINISTRATION Amount of Local Anesthetic Administered Dose of OraVerse 1 / 4 Cartridge 1 / 4 Cartridge (0.1 mg) ½ Cartridge ½ Cartridge (0.2 mg) 1 Cartridge 1 Cartridge (0.4 mg) 2 Cartridges 2 Cartridges (0.8 mg) OraVerse is administered using the same location(s) and same technique(s) (infiltration or block injection) used for the administration of local anesthetic.

Source: US FDA prescribing information

Contraindications

4. CONTRAINDICATIONS OraVerse is contraindicated in patients with: Hypersensitivity to the active substance or to any ingredients in the formulation OraVerse is contraindicated in patients with: Hypersensitivity to the active substance or to any ingredients in the formulation.

Source: US FDA prescribing information

Warnings and precautions

5. WARNINGS AND PRECAUTIONS Myocardial infarction, cerebrovascular spasm, and cerebrovascular occlusion have been reported to occur following the intravenous or intramuscular administration of phentolamine, usually in association with marked hypotensive episodes or shock-like states which occasionally follow parenteral administration. Tachycardia and cardiac arrhythmiasmay occur with the use of phentolamine or other alpha-adrenergic blocking agents.

Source: US FDA prescribing information

Side effects

6. ADVERSE REACTIONS In clinical trials, the most common adverse reaction with OraVerse that was greater than the control group was injection site pain. The most common adverse reaction with OraVerse (incidence ≥5% and > control) is injection-site pain.

Source: US FDA prescribing information

Interactions

7. DRUG INTERACTIONS There are no known drug interactions with OraVerse. Lidocaine and Epinephrine When OraVerse was administered as an intraoral submucosal injection 30 minutes after injection of a local anesthetic, 2% lidocaine HCl with 1:100,000 epinephrine, the lidocaine concentration increased immediately after OraVerse intraoral injection. Lidocaine AUC and Cmax values were not affected by administration of OraVerse. OraVerse administration did not affect the PK of epinephrine.

Source: US FDA prescribing information

Storage

Store at controlled room temperature, 20-25°C (68-77°F) with brief excursions permitted between 15-30°C (59-86°F) Protect from direct heat and light. Do not permit to freeze.

Source: US FDA prescribing information

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

All presentations

4 presentations of Phentolamine, sorted by availability.

MedicineManufacturerRegisterAvailability
Phentolamine 5 mg/mL powder for injectionIntramuscular, intravenousGeneric name—US FDAAvailable on request
Oraverse 0.3995 mg/1.7 mL injectionSubmucosalSeptodontUS FDAAvailable on request
Phentolamine 5 mg injectionIntramuscular, intravenousGeneric name—US FDAAvailable on request
Ryzumvi 10 mg/mL eye dropsOphthalmic Cold chainOyster Point PharmaUS FDAAvailable on request

Brands by market

2 brand names across 1 markets.

Brand names by country

United States

Manufacturers

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 30 January 1952Drugs@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 Phentolamine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Phentolamine available for export from India?

Yes, on request. MedsAcross lists 4 presentations of Phentolamine and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Phentolamine have?

The catalogue lists 2 brand names for Phentolamine, including Oraverse, Ryzumvi.

Is Phentolamine approved by the US FDA?

Yes. The US FDA first approved Phentolamine on 30 January 1952, according to Drugs@FDA.

Does Phentolamine need cold chain shipping?

At least one listed presentation of Phentolamine must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

Which ATC class is Phentolamine in?

Phentolamine is classified under ATC code C04AB01 (Phentolamine).

References

  1. Oraverse prescribing information (Septodont). U.S. National Library of Medicine, DailyMed. Retrieved 5 December 2018

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