Drug profile · INN
tenofovir disoproxil
TENOFOVIR ARX
tenofovir disoproxil (TENOFOVIR ARX) is an FDA-listed pharmaceutical active ingredient. Associated with Alphapharm Pty Ltd.
Drug details — tenofovir disoproxil
- Class
- Antiinfectives for systemic use (J05)
- Route
- —
- Patents
- 20
- Programs
- 17
- Data quality
- 0.83
Quick answer
tenofovir disoproxil (TENOFOVIR ARX) is an FDA-listed pharmaceutical active ingredient. Associated with Alphapharm Pty Ltd.
Key facts
Approval history
| Authority | Status | Date |
|---|---|---|
| EMA | approved | — |
| TGA | approved | — |
Pipeline programs
Related & competitor drugs
Related patents
-
US 12384779
Bicyclic compounds
granted -
US 12180192
Modulators of THR-β and methods of use thereof
granted -
US 12018015
Methods and compositions for targeting PD-L1
granted -
US 11957683
Bicyclic compounds
granted -
US 11952374
Bicyclic compounds
granted -
US 11939581
Methods and compositions for targeting PD-L1
granted -
US 11858913
Bicyclic pyridazinones and methods of use thereof
granted -
US 11840532
Modulators of THR-β and methods of use thereof
granted -
US 11820773
Tricyclic compounds
granted -
US 11793815
Oxindoles and methods of use thereof
granted -
US 11786532
2-pyridones and methods of use thereof
granted -
US 11771680
Pyrrole compounds
granted -
US 11760764
Methods and compositions for targeting PD-L1
granted -
US 11760761
Methods and compositions for targeting PD-L1
granted -
US 11613750
Methods of reducing virus molecule levels
granted -
US 11591341
Bicyclic and tricyclic compounds
granted -
US 11464783
Heterocyclic compounds
granted -
US 11198699
Compounds targeting PRMT5
granted -
US 11191747
Pyrrole compounds
granted -
US 11136321
Tricyclic compounds
granted
Frequently asked questions
What is tenofovir disoproxil?
tenofovir disoproxil (TENOFOVIR ARX) is an FDA-listed pharmaceutical active ingredient. Associated with Alphapharm Pty Ltd.
What is the brand name for tenofovir disoproxil?
TENOFOVIR ARX is a marketed brand name for tenofovir disoproxil. Check FDA Drugs@FDA for the current US label holder and prescribing information.