Urso 250 Oral Tablet 250Mg Drug Medication Dosage Information
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Urso 250: Oral tablet (250mg)

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Drug Image file DrugItem_1679.JPG
Urso-250 250mg Tab
Actavis- US Brands formerly Aptalis Pharma, a wholly owned subsidiary of Forest, Formerly Axcan Pharma US, Inc.
Pill Identification: URS 785 
Drug Image file DrugItem_11808.JPG
Ursodiol 250mg Tab
Prasco Laboratories
Pill Identification: URS 785 
Drug Image file DrugItem_17453.JPG
Ursodiol 250mg Tab
Actavis Inc. formerly Watson Pharmaceuticals Inc
Pill Identification: 2368 
Drug Image file DrugItem_19719.JPG
Ursodiol 250mg Tab
Par Pharmaceutical Inc
Pill Identification: LOGO 256 
Drug Image file DrugItem_17933.JPG
Ursodiol 250mg Tab
Blue Point Laboratories
Pill Identification: 2368 
Drug Image file DrugItem_18357.JPG
Ursodiol 250mg Tab
Global Pharmaceuticals
Pill Identification: 2368 

What is this Medicine?

URSODIOL (ER soe dye ol) helps dissolve gallstones in patients who cannot have or who do not need gallbladder surgery. This medicine is also useful for certain liver diseases of adults, children and infants.

In-Depth Information

Urso-250 250mg Tablet

NDC: 589140785
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Biliary Cirrhosis

Sometimes used for but not FDA approved for the following conditions:
Pruritus, Intrahepatic Cholestasis Of Pregnancy (ICP), Cystic Fibrosis, Non-alcoholic Steatosis-hepatitis (NASH)

Storage Information
Store at controlled room temperature (between 68 and 77 degrees F)
Urso-250 250mg Tablet
Drug Image file DrugItem_1679.JPG
Actavis- US Brands formerly Aptalis Pharma, a wholly owned subsidiary of Forest, Formerly Axcan Pharma US, Inc.
Pill Identification: URS 785 
Shape: oval
Color: white

Reported Side Effects for Urso-250 250mg Tablet

Vomiting Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Low Platelet Count Incidence:
1.3%*
Severity: MODERATE
Onset: DELAYED
Itching Incidence:
5.0%*
Severity: MILD
Onset: RAPID
Upset Stomach Incidence:
8.3%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
10.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


Learning More About
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