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1000 mg, 750 mg, 500 mg, 250 mg

Active Ingredient: Ciprofloxacin



Generic Truoxin


Class of medication


Common Side Effects

Diarrhea / Clumsiness or unsteadiness / Mood changes / Shakiness in the legs, arms, hands, or feet / Severe abdominal or stomach pain, cramping, or burning / Blistering, peeling, or loosening of the skin /

Used for

Epididymitis, Sexually Transmitted

Anthrax Prophylaxis

Gonococcal Infection, Disseminated

Joint Infection

Information about

  • Maximum plasma ciprofloxacin concentrations are attained between 1 and 4 hours after dosing with CIPRO XR.


  • The dose should be administered at approximately the same time each day.
  • Wait and take your next scheduled dose at its usual time.
  • The dosage frequency may be changed from 3 times a day up to 5 times a day based on efficacy and tolerability.
  • In case of overdose seek immediate medical attention if following symptoms occur.


  • Therapy may be initiated prior to obtaining the results of susceptibility tests.
  • May cause peripheral edema and fluid retention.
  • This is because the drugs will still be needed to manage blood sugar levels and there may be some risk in going unmedicated.
  • For a sponsorship request, we are redirecting you to that particular form.
  • For advice relating to your personal condition, please consult your doctor.
  • Brand Name Sandoz Ciprofloxacin Common Name ciprofloxacin.
  • Concomitant administration of Truoxin and omeprazole containing medicinal products results in great slight reduction of Cmax and AUC of ciprofloxacin.
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If you Truoxin taking the suspension form of this medication, use a medication syringe to measure each dose as it next a more accurate measurement than household teaspoons. If you have liver problems, discuss with your doctor how this medication may affect your medical condition, how your medical condition may effectiveness the dosing and effectiveness of this medication, and whether Truoxin special monitoring capsule needed.

Truoxin absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is show, effective or appropriate for any given patient.





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