SHORT DESCRIPTION
Stanozolol 10 is an oral androgen derived from dihydrotestosterone. Stanozolol 10 acts on
androgen receptors to promote anabolism through increased nitrogen retention and protein
synthesis in muscle tissue. Stanozolol 10 is a strong anabolic substance with androgenic
action. Stanozolol does not convert to estrogen and therefore does not produce typical
estrogen mediated side effects such as water retention. Stanozolol has a large oral
bioavailability, due to a C17 a-alkylation which allows the hormone to survive first pass liver
metabolism. Stanozolol reduces SHBG increasing free testosterone levels.
Stanozolol 50 is an aqueous suspension of the C17 a-alkylated steroid stanozolol, an oral
androgen derived from dihydro- testosterone. Stanozolol 50 acts on androgen receptors to
promote anabolism through increased nitrogen retention and protein synthesis in muscle
tissue. Stanozolol 50 is a strong anabolic substance with androgenic action. Stanozolol does
not convert to estrogen and therefore does not produce typical estrogen mediated side
effects such as water retention. While chemically identical to oral stanozolol, Stanozolol 50 is
injected IM eliminating the first pass of liver metabolism of its oral counterpart reducing
stress on the liver. Stanozolol reduces SHBG increasing free testosterone levels.