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Molecule

Methenamine

Also known as methenamine hippurate
Available on requestAntibiotics
Presentations
1
Brands
0
Manufacturers
0
Available from stock
0

Methenamine is a prescription medicine indicated for prophylactic or suppressive treatment of frequently recurring urinary tract infections when long-term therapy is considered necessary. It is available as tablets for oral use. MedsAcross supplies Methenamine 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

ATC classification
J01XX05 Methenamine · Antibiotics for systemic use, subgroup J01X, subgroup J01XX
US FDA first approval
5 July 1967
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Identifiers
UNII J50OIX95QVRxCUI 6832CAS 100-97-0DrugBank DB06799Q71969

Clinical information

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

Uses

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Methenamine Hippurate Tablets and other antibacterial drugs, Methenamine Hippurate Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Methenamine Hippurate Tablets are indicated for prophylactic or suppressive treatment of frequently recurring urinary tract infections when long-term therapy is considered necessary. This drug should only be used after eradication of the infection by other appropriate antimicrobial agents.

Source: US FDA prescribing information

Dosing overview

One tablet (1 g) twice daily for adults and children over 12 years of age. One-half tablet or one tablet (0.5 or 1 g) twice daily for children 6 to 12 years of age. The antibacterial activity of Methenamine Hippurate Tablets is greater in acid urine. Therefore, restriction of alkalinizing foods and medications is desirable. If necessary, as indicated by urinary pH and clinical response, supplemental acidification of the urine may be instituted. The efficacy of therapy should be monitored by repeated urine cultures.

Source: US FDA prescribing information

Contraindications

Methenamine Hippurate Tablets are contraindicated in patients with renal insufficiency, severe hepatic insufficiency, or severe dehydration. It should not be used as the sole therapeutic agent in acute parenchymal infections causing systemic symptoms.

Source: US FDA prescribing information

Warnings and precautions

Patients with pre-existing hepatic insufficiency may suffer adverse effects from the small amounts of ammonia and formaldehyde that are produced. The classical syndrome of acute hepatic failure may be evoked in these patients.

Source: US FDA prescribing information

Side effects

Adverse effects of Methenamine Hippurate Tablets have been reported in fewer than 3.5% of patients treated. These reactions have included the following, in decreasing order of frequency: nausea, vomiting and rarely pruritus, rash, dysuria. Children have received Methenamine Hippurate Tablets at the recommended dosages as a prophylactic/suppressive regimen after initial treatment of acute episodes of pyuria. Side effects were encountered in only 1.1% of these children.

Source: US FDA prescribing information

Interactions

The concomitant administration of methenamine hippurate and sulfamethizole or sulfathiazole is liable to result in the formation of a precipitate in the urine.

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 Methenamine, sorted by availability.

MedicineManufacturerRegisterAvailability
Methenamine 1 g tabletOralGeneric 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 5 July 1967Drugs@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 Methenamine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Methenamine available for export from India?

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

Is Methenamine approved by the US FDA?

Yes. The US FDA first approved Methenamine on 5 July 1967, according to Drugs@FDA.

Does Methenamine need cold chain shipping?

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

Which ATC class is Methenamine in?

Methenamine is classified under ATC code J01XX05 (Methenamine).

References

  1. Methenamine Hippurate prescribing information (Alvogen). U.S. National Library of Medicine, DailyMed. Retrieved 17 November 2024

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