| NDC Code | 69238-1549-3 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (69238-1549-3) |
|---|
| Product NDC | 69238-1549 |
|---|
| 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 | 133; 200 |
|---|
| 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] |
|---|