NDC Code | 60219-2092-3 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (60219-2092-3) |
Product NDC | 60219-2092 |
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 | 100; 150 |
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] |