Me NaPhos MB Hyo 1 URINARY ANTISEPTIC ANTISPASMODIC METHOD PHARMACEUTICALS FDA Approved Each tablet contains: Methenamine, USP ................................. 81.6 mg Monobasic Sodium Phosphate, USP ......... 40.8 mg Methylene Blue ....................................... 10.8 mg Hyoscyamine Sulfate ............................... 0.12 mg
FunFoxMeds bottle
Route
ORAL
Package NDC

Drug Facts

Composition & Profile

Inactive Ingredients
Inactive Ingredients include: Microcrystalline Cellulose Mannitol Croscarmellose Sodium Magnesium Stearate FD&C Blue #1 HYOSCYAMINE SULFATE is an alkaloid of belladonna. Exists as a white crystalline powder. Affected by light It is very soluble in water; freely soluble in alcohol; practically insoluble in ether. METHENAMINE exists as colorless lustrous crystals or white crystalline powder. Its solutions are alkaline to litmus. Freely soluble in water; soluble in alcohol and in chloroform. METHYLENE BLUE exists as dark green crystals. It is soluble in water and in chloroform; sparingly soluble in alcohol. MONOBASIC SODIUM PHOSPHAT E exists as a white crystalline powder. Its solutions are acidic to litmus. It is freely soluble in water and practically insoluble in alcohol. This product is not an Orange Book (OB) rated product therefore all prescriptions using this product shall be pursuant to state statutes as applicable. There are no claims of bioequivalence or therapeutic equivalence.
Quantities
1 tablets 100 tablets
Treats Conditions
Indication And Usage Me Naphos Mb Hyo 1 Tablets Is Indicated For The Treatment Of Symptoms Of Irritative Voiding Indicated For The Relief Of Local Symptoms Such As Hypermotility Which Accompany Lower Urinary Tract Infections And As Antispasmodic Indicated For The Relief Of Urinary Tract Symptoms Caused By Diagnostic Procedures
Pill Appearance
Shape: oval Color: blue Imprint: M455

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UPC
0358657454012
UNII
OB570Z127K J50OIX95QV 8NAP7826UB 593YOG76RN
Packaging

HOW SUPPLIED ME/NaPhos/MB/Hyo 1 Tablets are light blue to blue, oval, biconvex tablets debossed with "M455" with scoreline on one side and plain on the other side. Supplied in bottles of 100 tablets (NDC 58657-454-01).; Distributed by: Method Pharmaceuticals, LLC Arlington, TX 76006 Rev. Date: 01/2016 Pinciple Display Panel Booklet lab booklet

Package Descriptions
  • HOW SUPPLIED ME/NaPhos/MB/Hyo 1 Tablets are light blue to blue, oval, biconvex tablets debossed with "M455" with scoreline on one side and plain on the other side. Supplied in bottles of 100 tablets (NDC 58657-454-01).
  • Distributed by: Method Pharmaceuticals, LLC Arlington, TX 76006 Rev. Date: 01/2016 Pinciple Display Panel Booklet lab booklet

Overview

Each tablet contains: Methenamine, USP ................................. 81.6 mg Monobasic Sodium Phosphate, USP ......... 40.8 mg Methylene Blue ....................................... 10.8 mg Hyoscyamine Sulfate ............................... 0.12 mg

Indications & Usage

INDICATION AND USAGE ME/NaPhos/MB/Hyo 1 Tablets is indicated for the treatment of symptoms of irritative voiding. Indicated for the relief of local symptoms, such as hypermotility which accompany lower urinary tract infections and as antispasmodic. Indicated for the relief of urinary tract symptoms caused by diagnostic procedures.

Dosage & Administration

Adults One tablet orally 4 times per day followed by liberal fluid intake. Older Children Dosage must be individualized by physician. Not recommended for use in children up to 6 years of age.

Warnings & Precautions
WARNINGS Do not exceed recommended dosage. If rapid pulse, dizziness, or blurring of vision occurs discontinue use immediately.
Adverse Reactions

Cardiovascula r – rapid pulse, flushing Central Nervous System – blurred vision, dizziness Respiratory – shortness of breath or troubled breathing Genitourinary – difficulty micturition, acute urinary retention Gastrointestinal – dry mouth, nausea/vomiting

Drug Interactions

because of this product's effect on gastrointestinal motility and gastric emptying, it may decrease the absorption of other oral medications during concurrent use such as: urinary alkalizers; thiazide diuretics (may cause the urine to become alkaline reducing the effectiveness of methenamine by inhibiting its conversion to formaldehyde); antimuscarinics (concurrent use may intensify antimuscarinic effects of hyoscyamine because of secondary antimuscarinic activities of these medications); antacids/antidiarrheals (may reduce absorption of hyoscyamine, concurrent use with antacids may cause urine to become alkaline reducing effectiveness of methenamine by inhibiting its conversion to formaldehyde) doses of these medications should be spaced 1 hour apart from doses of hyoscyamine; antimyasthenics (concurrent use with hyoscyamine may further reduce intestinal motility); ketoconazole (patients should be advised to take this combination at least 2 hours after ketoconazole); monoamine oxidase (MAO) Inhibitors (concurrent use may intensify antimuscarinic side effects, opioid (narcotic) analgesics may result in increased risk of severe constipation); sulfonamides (these drugs may precipitate with formaldehyde in the urine, increasing the danger of crystalluria). Patients should be advised that the urine may become blue to blue green and the feces may be discolored as a result of the excretion of methylene blue.


Similar Drugs

Related medications based on brand, generic name, substance, active ingredients.

View all similar drugs →