SUSTIVA - 54868-4668-0 - (efavirenz)

Alphabetical Index


Drug Information of SUSTIVA

Product NDC: 54868-4668
Proprietary Name: SUSTIVA
Non Proprietary Name: efavirenz
Active Ingredient(s): 600    mg/1 & nbsp;   efavirenz
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SUSTIVA

Product NDC: 54868-4668
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021360
Marketing Category: NDA
Start Marketing Date: 20121011

Package Information of SUSTIVA

Package NDC: 54868-4668-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-4668-0)

NDC Information of SUSTIVA

NDC Code 54868-4668-0
Proprietary Name SUSTIVA
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-4668-0)
Product NDC 54868-4668
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name efavirenz
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121011
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name EFAVIRENZ
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of SUSTIVA


General Information