"72189-312-03" National Drug Code (NDC)

NDC Code	72189-312-03
Package Description	3 TABLET, FILM COATED in 1 BOTTLE (72189-312-03)
Product NDC	72189-312
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Emtricitabine And Tenofovir Disoproxil Fumarate
Non-Proprietary Name	Emtricitabine And Tenofovir Disoproxil Fumarate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20220126
Marketing Category Name	ANDA
Application Number	ANDA204131
Manufacturer	DirectRx
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]