Canephron N No. 60 dragee


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Canephron H No. 60 dragee

Canephron N dragee - a combined preparation of plant origin, has a diuretic, antispasmodic, anti-inflammatory, antimicrobial effect.

Pharmacotherapeutic group:

Herbal diuretic agent.


Orange, round, biconvex dragees with a smooth surface.

Indications for use:

The drug is used in the treatment of chronic infections of the bladder (cystitis) and kidneys (pyelonephritis), with non-infectious chronic inflammation of the kidneys (glomerulonephritis, interstitial nephritis), as a means of preventing the formation of urinary stones (also after removal of urinary stones).


Hypersensitivity to the drug. Children's age (up to 6 years). Peptic ulcer and duodenal ulcer in the acute stage. Lactase deficiency, lactose intolerance, glucose-galactose malabsorption. Deficiency of sucrase / isomaltase, fructose intolerance.

Use during pregnancy and during breastfeeding:

The use of the drug during pregnancy and during breastfeeding is possible only on prescription, in strict accordance with the recommendations for use and after evaluation by the attending physician of the risk-benefit ratio.

Side effect:

Allergic reactions are possible. Possible disorders of the gastrointestinal tract (nausea, vomiting, diarrhea).

If there are signs of an allergic reaction, you should stop taking the drug.


At present, there is no data on overdose and intoxication.

In case of drug overdose, symptomatic treatment is prescribed.

Interaction with other drugs:

Combination with antibacterial agents is possible and appropriate. Interactions with other drugs are currently unknown.

Special instructions:

For edema caused by impaired function of the heart or kidneys, the consumption of large amounts of fluid is contraindicated.

With impaired renal function, the drug should not be prescribed as monotherapy.In case of inflammatory kidney disease, you should consult a doctor for advice.

In the case of the presence of blood in the urine, pain during urination or in acute urinary retention, an urgent need to consult a doctor.

Digestible carbohydrates contained in one dragee, are less than 0.04 "bread units" (HE).

Impact on the ability to drive vehicles and mechanisms:

The drug does not affect the ability to perform potentially hazardous activities that require high concentration of attention and speed of psychomotor reactions (including driving and working with moving mechanisms).

Release form:

Dragee On 20 dragees in the blister from aluminum foil (lower part) and polyvinyl chloride / polyvinylidene chloride film (upper part). On 3 or 6 blisters together with the instruction for application are placed in a folding cardboard box.

Storage conditions:

Store in a dry, dark place at a temperature not exceeding 25 ° C.

Keep out of the reach of children.

Shelf life

3 years.

Do not use beyond the expiration date printed on the package.

Pharmacy sales terms

Over the counter.

It is a pharmaceutical drug. Use only as directed by your doctor.


Active ingredients:

crushed medicinal plant raw materials:

  • Centaury grass
18 mg
  • Lovable medicinal root
18 mg
  • Rosemary leaves
18 mg
  • Excipients:
  • Corn starch
15 mg
  • Colloidal silicon dioxide
5.5 mg
  • Lactose monohydrate
45.0 mg
  • Povidone
9.0 mg
  • Shell:
  • Iron oxide red
0.049 mg
  • Riboflavin E 101
0.243 mg
  • Calcium carbonate
17,222 mg
  • Dextrose
0.972 mg
  • Corn starch
2,500 mg
  • Modified corn starch
2.140 mg
  • Mountain glycolic wax
0.075 mg
  • Povidone
0.103 mg
  • Castor oil
0.025 mg
  • Sucrose
57.182 mg
  • Shellac
0.615 mg
  • Talc
43.541 mg
  • Titanium dioxide
0.333 mg

Mode of application

Inside, without chewing, drinking water. Adults: 2 pills 3 times a day. School children: 1 tablet 3 times a day. After weakening the severity of the disease should continue treatment with the drug for 2 to 4 weeks.

A large amount of fluid is recommended during drug treatment.