Ursodiol - 68462-474-01 - (Ursodiol)

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Drug Information of Ursodiol

Product NDC: 68462-474
Proprietary Name: Ursodiol
Non Proprietary Name: Ursodiol
Active Ingredient(s): 500    mg/1 & nbsp;   Ursodiol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ursodiol

Product NDC: 68462-474
Labeler Name: Glenmark Generics Inc.,USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090801
Marketing Category: ANDA
Start Marketing Date: 20110712

Package Information of Ursodiol

Package NDC: 68462-474-01
Package Description: 100 TABLET in 1 BOTTLE (68462-474-01)

NDC Information of Ursodiol

NDC Code 68462-474-01
Proprietary Name Ursodiol
Package Description 100 TABLET in 1 BOTTLE (68462-474-01)
Product NDC 68462-474
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ursodiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110712
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc.,USA
Substance Name URSODIOL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient]

Complete Information of Ursodiol


General Information