| NDC Code | 65862-820-03 |
|---|
| Package Description | 3 BLISTER PACK in 1 CARTON (65862-820-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 65862-820 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tenofovir Disoproxil Fumarate |
|---|
| Non-Proprietary Name | Tenofovir Disoproxil Fumarate |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180126 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090647 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | TENOFOVIR DISOPROXIL FUMARATE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS] |
|---|