URSO - 55154-1855-4 - (ursodiol)

Alphabetical Index


Drug Information of URSO

Product NDC: 55154-1855
Proprietary Name: URSO
Non Proprietary Name: ursodiol
Active Ingredient(s): 250    mg/1 & nbsp;   ursodiol
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of URSO

Product NDC: 55154-1855
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020675
Marketing Category: NDA
Start Marketing Date: 19971210

Package Information of URSO

Package NDC: 55154-1855-4
Package Description: 100 POUCH in 1 CARTON (55154-1855-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-1855-6)

NDC Information of URSO

NDC Code 55154-1855-4
Proprietary Name URSO
Package Description 100 POUCH in 1 CARTON (55154-1855-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-1855-6)
Product NDC 55154-1855
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ursodiol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19971210
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name URSODIOL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient]

Complete Information of URSO


General Information