Truvada - 52959-969-03 - (emtricitabine and tenofovir disoproxil fumarate)

Alphabetical Index


Drug Information of Truvada

Product NDC: 52959-969
Proprietary Name: Truvada
Non Proprietary Name: emtricitabine and tenofovir disoproxil fumarate
Active Ingredient(s): 200; 300    mg/1; mg/1 & nbsp;   emtricitabine and tenofovir disoproxil fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Truvada

Product NDC: 52959-969
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021752
Marketing Category: NDA
Start Marketing Date: 20040802

Package Information of Truvada

Package NDC: 52959-969-03
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-969-03)

NDC Information of Truvada

NDC Code 52959-969-03
Proprietary Name Truvada
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-969-03)
Product NDC 52959-969
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name emtricitabine and tenofovir disoproxil fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040802
Marketing Category Name NDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength Number 200; 300
Strength Unit mg/1; mg/1
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Truvada


General Information