"16714-534-01" National Drug Code (NDC)

NDC Code	16714-534-01
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (16714-534-01)
Product NDC	16714-534
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	20220309
Marketing Category Name	ANDA
Application Number	ANDA203442
Manufacturer	NorthStar RxLLC
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]