TEMODAR - 54868-4142-3 - (Temozolomide)

Alphabetical Index


Drug Information of TEMODAR

Product NDC: 54868-4142
Proprietary Name: TEMODAR
Non Proprietary Name: Temozolomide
Active Ingredient(s): 20    mg/1 & nbsp;   Temozolomide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of TEMODAR

Product NDC: 54868-4142
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021029
Marketing Category: NDA
Start Marketing Date: 20050629

Package Information of TEMODAR

Package NDC: 54868-4142-3
Package Description: 60 CAPSULE in 1 BOTTLE (54868-4142-3)

NDC Information of TEMODAR

NDC Code 54868-4142-3
Proprietary Name TEMODAR
Package Description 60 CAPSULE in 1 BOTTLE (54868-4142-3)
Product NDC 54868-4142
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Temozolomide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050629
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TEMOZOLOMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of TEMODAR


General Information