NDC Code | 53808-1128-1 |
Package Description | 30 TABLET in 1 BLISTER PACK (53808-1128-1) |
Product NDC | 53808-1128 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Tenofovir Disoproxil Fumarate |
Non-Proprietary Name | Tenofovir Disoproxil Fumarate |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20180424 |
Marketing Category Name | ANDA |
Application Number | ANDA090742 |
Manufacturer | DOH CENTRAL PHARMACY |
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] |