-
Dihydrotestosterone
- indication:
- pharmacologypharmacology:
- mechanism:
- toxicity: Oral LD<sub>50</sub> in rat is 7060 mg/kg. Oral LD<sub>50</sub> in mouse is 3450 mg/kg.
- absorprion: Bioavailability is very low (0-2%) following oral administration.
- halflife:
- roouteelimination:
- volumedistribution:
- clearance: