"67296-1237-3" National Drug Code (NDC)

NDC Code	67296-1237-3
Package Description	3 TABLET, FILM COATED in 1 BOTTLE (67296-1237-3)
Product NDC	67296-1237
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Truvada
Non-Proprietary Name	Truvada
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20040802
Marketing Category Name	NDA
Application Number	NDA021752
Manufacturer	RedPharm Drug, Inc.
Substance Name	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength	200; 300
Strength Unit	mg/1; mg/1
Pharmacy Classes	Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS], Nucleosides [CS]