| NDC Code | 60219-2094-3 | 
|---|
			| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (60219-2094-3) | 
|---|
			| Product NDC | 60219-2094 | 
|---|
			| 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 | 20180826 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA209721 | 
|---|
			| Manufacturer | Amneal Pharmaceuticals NY LLC | 
|---|
			| Substance Name | EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE | 
|---|
			| Strength | 167; 250 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA] | 
|---|