Ursodiol - 0591-2368-01 - (Ursodiol)

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Drug Information of Ursodiol

Product NDC: 0591-2368
Proprietary Name: Ursodiol
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 Ursodiol

Product NDC: 0591-2368
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200826
Marketing Category: ANDA
Start Marketing Date: 20111223

Package Information of Ursodiol

Package NDC: 0591-2368-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-2368-01)

NDC Information of Ursodiol

NDC Code 0591-2368-01
Proprietary Name Ursodiol
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-2368-01)
Product NDC 0591-2368
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ursodiol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111223
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name URSODIOL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient]

Complete Information of Ursodiol


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