Tasmar - 0187-0938-07 - (Tolcapone)

Alphabetical Index


Drug Information of Tasmar

Product NDC: 0187-0938
Proprietary Name: Tasmar
Non Proprietary Name: Tolcapone
Active Ingredient(s): 100    mg/1 & nbsp;   Tolcapone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tasmar

Product NDC: 0187-0938
Labeler Name: Valeant Pharmaceuticals North America LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020697
Marketing Category: NDA
Start Marketing Date: 20040727

Package Information of Tasmar

Package NDC: 0187-0938-07
Package Description: 21 TABLET, FILM COATED in 1 BOTTLE (0187-0938-07)

NDC Information of Tasmar

NDC Code 0187-0938-07
Proprietary Name Tasmar
Package Description 21 TABLET, FILM COATED in 1 BOTTLE (0187-0938-07)
Product NDC 0187-0938
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tolcapone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040727
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America LLC
Substance Name TOLCAPONE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC]

Complete Information of Tasmar


General Information