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MedsAcross

Molecule

Mebendazole

Anthelmintic
Available on requestOrphan
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Mebendazole is an anthelmintic indicated for the treatment of patients one year of age and older with gastrointestinal infections caused by Ascaris lumbricoides (roundworm) and Trichuris trichiura (whipworm). It is available as chewable tablets for oral use. MedsAcross supplies Mebendazole 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
Anthelmintic
ATC classification
P02CA01 Mebendazole · Antinematodal agent, subgroup P02CA
US FDA first approval
28 June 1974
EU status
Not recorded
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Chewable tablet
Identifiers
UNII 81G6I5V05IRxCUI 6672CAS 31431-39-7DrugBank DB00643Q422194

Clinical information

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

Uses

VERMOX™ CHEWABLE is indicated for the treatment of patients one year of age and older with gastrointestinal infections caused by Ascaris lumbricoides (roundworm) and Trichuris trichiura (whipworm). VERMOX™ CHEWABLE is an anthelmintic indicated for the treatment of patients one year of age and older with gastrointestinal infections caused by: Ascaris lumbricoides (roundworm) and Trichuris trichiura (whipworm).

Source: US FDA prescribing information

Dosing overview

The recommended dosage in patients one year of age and older is one VERMOX™ CHEWABLE 500 mg tablet taken as a single dose. Chew VERMOX™ CHEWABLE 500 mg tablet completely before swallowing. Do not swallow the tablet whole. For patients who have difficulty chewing the tablet, approximately 2 mL to 3 mL of drinking water can be added to a suitably sized spoon and the VERMOX™ CHEWABLE 500 mg tablet placed into the water. Within 2 minutes, the tablet absorbs the water and turns into a soft mass with semi-solid consistency, which can then be swallowed. VERMOX™ CHEWABLE 500 mg tablet can be taken without regard to food intake. The recommended dosage in patients one year of age and older is one single tablet of VERMOX™ CHEWABLE 500 mg taken as a single dose, chewed completely before swallowing.

Source: US FDA prescribing information

Contraindications

VERMOX™ CHEWABLE is contraindicated in persons with a known hypersensitivity to the drug or its excipients. Patients with a known hypersensitivity to the drug or its excipients

Source: US FDA prescribing information

Warnings and precautions

Risk of Convulsions: Convulsions in infants below the age of 1 year have been reported. Hematologic Effects: Neutropenia and agranulocytosis have been reported in patients receiving mebendazole at higher doses and for prolonged duration. Monitor blood counts in these patients. Metronidazole and Serious Skin Reactions: Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) have been reported with the concomitant use of mebendazole and metronidazole. Avoid concomitant use of mebendazole and metronidazole

Source: US FDA prescribing information

Side effects

Adverse reactions reported in clinical trials were anorexia, abdominal pain, diarrhea, flatulence, nausea, vomiting and rash.

Source: US FDA prescribing information

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

All presentations

1 presentations of Mebendazole, sorted by availability.

MedicineManufacturerRegisterAvailability
Vermox 500 mg chewable tabletOralJanssen PharmaceuticalsUS FDAAvailable on request

Brands by market

1 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 28 June 1974Drugs@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 Mebendazole in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Mebendazole available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Mebendazole and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Mebendazole have?

The catalogue lists 1 brand names for Mebendazole, including Vermox.

Is Mebendazole approved by the US FDA?

Yes. The US FDA first approved Mebendazole on 28 June 1974, according to Drugs@FDA.

Does Mebendazole need cold chain shipping?

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

Which ATC class is Mebendazole in?

Mebendazole is classified under ATC code P02CA01 (Mebendazole).

References

  1. VERMOX prescribing information (Janssen Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 5 October 2021

Request Mebendazole for export supply

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