Methenamine Hippurate METHENAMINE HIPPURATE ALVOGEN INC. FDA Approved Methenamine Hippurate Tablets are a urinary tract antiseptic drug. Each white, scored tablet contains methenamine hippurate 1g (see HOW SUPPLIED). Methenamine Hippurate Tablets also contain: magnesium stearate, povidone and saccharin sodium. Chemically, methenamine hippurate is the hippuric acid salt of methenamine (hexamethylenetetramine). Structural formula: C 15 H 21 N 5 O 3 Molecular Weight 319.37 Methenamine structural formula
FunFoxMeds bottle
Route
ORAL
Applications
NDA016151
Package NDC

Drug Facts

Composition & Profile

Strengths
1 g
Quantities
100 tablets
Treats Conditions
Indications And Usage 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

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
M329791L57
Packaging

HOW SUPPLIED Methenamine Hippurate Tablets are capsule-shaped, scored, white, debossed “CL 20” on one side. Each tablet contains methenamine hippurate 1 g. Bottles of 100 tablets (NDC 47781-577-01). Store at controlled room temperature 15°-30°C (59°-86°F).; PACKAGE/LABEL PRINCIPAL DISPLAY PANEL NDC 47781- 577 -01 Methenamine Hippurate Tablets 1g Rx only 100 Tablets

Package Descriptions
  • HOW SUPPLIED Methenamine Hippurate Tablets are capsule-shaped, scored, white, debossed “CL 20” on one side. Each tablet contains methenamine hippurate 1 g. Bottles of 100 tablets (NDC 47781-577-01). Store at controlled room temperature 15°-30°C (59°-86°F).
  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL NDC 47781- 577 -01 Methenamine Hippurate Tablets 1g Rx only 100 Tablets

Overview

Methenamine Hippurate Tablets are a urinary tract antiseptic drug. Each white, scored tablet contains methenamine hippurate 1g (see HOW SUPPLIED). Methenamine Hippurate Tablets also contain: magnesium stearate, povidone and saccharin sodium. Chemically, methenamine hippurate is the hippuric acid salt of methenamine (hexamethylenetetramine). Structural formula: C 15 H 21 N 5 O 3 Molecular Weight 319.37 Methenamine structural formula

Indications & Usage

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.

Dosage & Administration

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.

Warnings & Precautions
WARNINGS 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.
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.

Adverse Reactions

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.

Drug Interactions

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


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