| NDC Code | 69076-105-03 |
|---|
| Package Description | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (69076-105-03) |
|---|
| Product NDC | 69076-105 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tenofovir Disoproxil Fumarate |
|---|
| Non-Proprietary Name | Tenofovir Disoproxil Fumarate |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209498 |
|---|
| Manufacturer | Quinn Pharmaceuticals |
|---|
| Substance Name | TENOFOVIR DISOPROXIL FUMARATE |
|---|
| Strength | 300 |
|---|
| 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] |
|---|