CAS Name: (11b,17b)-9-Fluoro-11,17-dihydroxy-17-methylandrost-4-en-3-one Halotestex Fluoxymesterone is a 17-alpha-alkylated oral anabolic-androgenic steroid. Halogenation at position 9 increases the pharmacologic activity per unit weight compared to testosterone when given orally and reduces aromatization. It is a strong androgen with limited anabolic activity. Fluoxymesterone can be reduced by 5-alpha reductase into DHT and some of it's androgenic activity may be caused not by fluoxymesterone itself, but to its metabolite DHT. Indication males: Fluoxymesterone used in hypogonadal males to induce normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. Effects also include growth and maturation of prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement; vocal cord thickening; alterations in body musculature; and fat distribution. Therefore, main indications for fluoxymesterolone are: primary hypogonadism (congenital or acquired) - testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, or orchidectomy; hypogonadotropic hypogonadism (congenital or acquired) - idiopathic gonadotropin or luteinizing hormone-releasing hormone (LHRH) deficiency, or pituitary-hypothalamic injury from tumors, trauma, or radiation. Indication females: Metastatic mammary cancer - may be used secondarily in women with advancing inoperable metastatic (skeletal) mammary cancer who are one to five years postmenopausal. Primary goals of therapy in these women include ablation of the ovaries. each tablet contains: Fluoxymesterone USP 10 mg Excipients q.s.

CAS Name: (17b)-17-Hydroxy-17-methylandrosta-1,4-dien-3-one Methanabol Methandrostenolone is a 17-alpha-alkylated oral anabolic-androgenic steroid with anabolic properties that are more pronounced than its androgenic effects. It has little progestational activity and easily converts to estrogens. Methandrostenolone has an anabolic activity index 0.60 and an androgenic activity index 0.20. Methandrostenolone has an extra double bond in the A-ring and, therefore, is not converted by 5-alpha reduction into DHT. Since methandrostenolone was created in the 1960s, it has been used for many different applications. At present, the only legitimate therapeutic indications for this anabolic steroid are: replacement of male sex steroids in men who have androgen deficiency, for example as a result of loss of both testes; the treatment of certain rare forms of aplastic anemia which are or may be responsive to anabolic androgens; and, in certain countries, to counteract catabolic states, for example after major trauma. each tablet contains: Methandrostenolone BP 10 mg

CAS Name: (5a,17b)-17-Hydroxy-17-methyl-2-oxaandrostan-3-one Oxanabol Oxandrolone is a 17-alpha-alkylated oral anabolic steroid. Oxandrolone has an excellent myotrophic activity index of 3.2 and a low androgenic activity index of 0.2. At low doses, oxandrolone will not cause suppression of endogenous testosterone production and does not aromatize to estrogens. Oxandrolone was approved for treating alcoholic hepatitis, Turner's syndrome, and weight loss caused by HIV. In addition, the drug has shown positive results in treating anemia and hereditary angioedema and for preserving muscle mass in burns patients. Oxandronolne also has been used with good success for idiopathic muscle mass loss and osteoporosis. At low dose (5-10mg), oxandrolone binds weakly to androgen receptors and therefore can be used by woman and does not cause virilisation. Oxandrolone has a half life 10-13 hours.

CAS Name: (5a,17b)-17-Hydroxy-2-(hydroxymethylene)-17-methylandrostan-3-one Oxydrol Oxymetholone is a 17-alpha-alkylated oral anabolic-androgenic steroid. Oxymetholone is very effective in promoting muscle gains and has an excellent myotrophic activity index of 3.2 and is similar to testosterone with an androgenic activity index of 0.45. Main clinical uses include: osteoporosis, anemia, as well as stimulating muscle growth in undernourished or underdeveloped patients. Also, oxymetholone has been studied for the treatment of HIV-associated wasting, antithrombin III deficiency, pediatric growth impairment, and damaged myocardium, with varying degrees of success. each tablet contains: Oxymetholone BP 50 mg

CAS Name: 17beta-Hydroxy-1-methyl-5alpha-androst-1-en-3-one acetate Primobol Methenolone acetate is an oral steroid derivative of dihydrotestosterone (DHT) with a mild myotrophic activity index 0.85 and a low androgenic index 0.12. Methenolone acetate is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces stress on the liver, but also this steroid's bioavailability. It is considered one of the safer steroids, meaning it has few side effects. Because of it's low androgenic activity, methenolone acetate does not suppress endogenous testosterone secretion. Methenolone is also not overly suppressive of the HPTA axis, but will become suppressive with increased doses.

CAS Name: (5a,17b)-17-Methyl-2'H-androst-2-eno[3,2-c]pyrazol-17-ol Stanabol Stanozolol is a17-alpha-alkylated anabolic steroid with good oral bioavailability. While stanazolol’s androgenic activity index of stanozolol is nearly the same as testosterone, its myotrophic activity is much higher at 2.0–3.7. Stanozolol does not aromatize and does not cause water retention. Stanozolol has been used for weight loss management in HIV patients with chronic obstructive pulmonary disease and has showed significant improvement in weight, body mass index, LBM, and muscle size. Stanozolol has been shown in vitro to significantly enhance collagen synthesis. A positive effect of stanazolol on wound healing in patients with non-healing wounds has also been demonstrated. Clinical studies show that the treatment with stanozolol during the induction phase of chemotherapy results in a positive effect on the duration of cancer-free remission. each tablet contains: Stanozolol USP 10 mg

CAS Name: 4-chloro-17a-methyl-17b-hydroxyandrosta-1,4-dien-3-one Turanabol Chlorodehydromethyltestosterone is an oral 17-alpha-alkylated steroid with a low androgenic acivity index 0.10-0.15 similar to methenolone and a myotrophic activity index of 0.50. Because of the 4-chloro alteration, chlorodehydromethyltestosterone does not convert into estrogens nor into DHT. Chlorodehydromethyltestosterone is used in cases of muscle wasting syndrome in HIV patients. Because of it's low androgenic activity chlorodehydromethyltestosterone can be used by woman and does not cause virilization. Chlorodehydromethyltestosterone on low doses does not suppressive on hypothalamic-pituitary axis (HTPA) function. each tablet contains: Chlorodehydromethyteststerone 10 mg

CAS Name: (17b)-17-Hydroxyandrost-4-en-3-one Aquabol Testosterone suspension is an injectable preparation containing unesterfied testosterone in a water base. Testosterone suspension is one of the oldest forms of testosterone. It differs from the other testosterone in that is dissolved in water, giving it some unique properties. The most significant one is that it is absorbs very quickly and starts to have an effect in 1-2 hours after injecting. Very fast acting, testosterone suspension will sustain elevated testosterone levels for 1- 2 days only. This drug requires frequent injections. The testosterone in this compound will convert easily easily into dihydrotestosterone and estogens. each mL contains: Testosterone Suspension USP 100 mg Benzyl Alcohol BP 0.9% v/v Carmellose Sodium BP 0.1% w/v Water for Injections BP q.s.

CAS Name: 1,4-androstadiene-3-one,17?-ol Boldabol Boldenone undecylenate is a derivative of testosterone with similar androgenic activity and higher mytrophic activity. Boldenone undecylenate does not convert into estrogens and does not have estrogen-related side effects. Instead, boldenone undecylenate is converted by 5-alpha-reductase into dihydroboldenone and some of it's androgenic effect mediated by dihydroboldenone. Boldenone undecylenate increases overall body metabolism rate and increases appetite. Increase in lean body mass and low side effects make this anabolic/androgenic steroid (AAS) a good therapeutic choice for age-related non-genomic muscle degenerative diseases like sarcopenia. The undecylenate ester extends half-life of boldenone in circulation, which, depending on dose, is approximately seven days.

CAS Name: (17b)-17-Hydroxyestr-4-en-3-one Decabol Nandrolone decanoate is an injectable anabolic androgenic steroid. It is indicated for the management of the anemia of renal insufficiency and has been shown to increase hemoglobin and red cell mass. Nandrolone cannot be reduced by 5-alpha reductase into DHT and therefore does not have an adverse reaction on the prostate. Instead of DHT, nandrolone metabolizes into dihydronandrolone. Nandrololone does not convert into estrogens. Nandrolone binds well to androgen receptors and also possesses non-receptor mediated stimulation on muscle growth. Nandrolone decanoate is one of the most potent anabolic steroid sfor muscle growth with an excellent myotrophic activity index 3.29–4.92. Nandrolone up-regulates androgen receptor AR expression in skeletal muscle, thus potentiating the actions of other steroids. Nandrolone does not have alkylation on the 17?-carbon and therefore is not toxic for the liver. each mL contains: Nandrolone Decanoate BP 200 mg Benzyl Alcohol BP 2% v/v Arachis Oil BP q.s.

Durabol Inject General information: CAS Name: 3-Oxoestr-4-en-17beta-yl 3-phenylpropionate Durabol Nandrolone phenylpropionate is an injectable anabolic androgenic steroid. It is attached to a short ester. It is indicated for the management of the anemia of renal insufficiency and has been shown to increase hemoglobin and red cell mass. Nandrolone cannot be reduced by 5-alpha reductase into DHT and therefore does not have an adverse reaction on the prostate. Instead of DHT, nandrolone metabolizes into dihydronandrolone. Nandrololones does not convert into estrogens. Nandrolone binds well to androgen receptors and also possesses non-receptor mediated stimulation on muscle growth. Nandrolone phenylpropionate is one of the most potent anabolic steroid for muscle growth with an excellent myotrophic activity index of 3.29–4.92. Nandrolone up-regulates androgen receptor AR expression in skeletal muscle, thus potentiating the actions of other steroids. Nandrolone does not have alkylation on the 17?-carbon and therefore is not toxic to the liver.

Dynabol Inject General information: CAS Name: 17beta-Hydroxyestr-4-en-3-one 17-undecanoate Dynabol Nandrolone undecanoate is an injectable anabolic androgenic steroid. It is indicated for the management of the anemia of renal insufficiency and has been shown to increase hemoglobin and red cell mass. Nandrolone cannot be reduced by 5-alpha reductase into DHT and therefore does not have an adverse reaction on the prostate. Instead of DHT, nandrolone metabolizes into dihydronandrolone. Nandrololone does not convert into estrogens. Nandrolone binds well to androgen receptors and also possesses non-receptor mediated stimulation on muscle growth. Nandrolone undecanoate one of the most potent anabolic steroid for muscle growth with an excellent myotrophic activity index 3.29–4.92. Nandrolone up-regulates androgen receptor AR expression in skeletal muscle, thus potentiating the actions of other steroids. Nandrolone does not have alkylation on the 17?-carbon and therefore is not toxic to the liver. each mL contains: Nandrolone undecanoate 200 mg Benzyl Alcohol BP 2% v/v Arachis Oil BP q.s.

Mastabol Inject General information: CAS Name: 17 beta-hydroxy-2 alpha-methyl-5 alpha-androstan-3-one Mastabol Drostanolone propionate is an injectable anabolic/androgenic steroid (AAS). It is highly androgenic and mildly anabolic. Drostanolone does not aromatize into estrogens and has similar properties to dihydrotestosterone (DHT). Drostanolone originally was developed to be used as an anti-estrogenic compound for treating female breast cancer. Drostanolone is irreversibly metabolized by the enzyme 3a-hydroxysteroid-dehydrogenase into an inactive form of 2?-methyl-5?-androstan-3?-ol-17-one. each mL contains: Drostanolone Propionate 100 mg Benzyl Alcohol BP 2% v/v Arachis Oil BP q.s.

Primobol Inject General information: CAS Name: (5?,17?)-1-methyl-3-oxoandrost-1-en-17-yl heptanoate Primobol Methenolone enanthate is an injectable steroid derivative of dihydrotestosterone (DHT) with a mild myotrophic activity index 0.85 and a low androgenic index 0.12. It's half-life dose dependent and is generally about 5 days. Methenolone is considered one of the safer steroids, meaning it has few side effects. Methenolone, because of it's low androgenic activity does not suppress endogenous testosterone secretion. Methenolone also is not overly suppressive of the hypothalamic-pituitary axis (HPTA), but will become suppressive with increased doses. each mL contains: Methanolon Enanthate 100mg Benzyl Alcohol BP 2% v/v Arachis Oil BP q.s.

Stanabol Inject General information: CAS Name: (5a,17b)-17-Methyl-2'H-androst-2-eno[3,2-c]pyrazol-17-o Stanabol Stanozolol is a17-alpha-alkylated anabolic steroid with good oral bioavailability. While stanazolol’s androgenic activity index of stanozolol is nearly the same as testosterone, its myotrophic activity is much higher at 2.0–3.7. Stanozolol does not aromatize and does not cause water retention. Stanozolol has been used for weight loss management in HIV patients with chronic obstructive pulmonary disease and has showed significant improvement in weight, body mass index, LBM, and muscle size. Stanozolol has been shown in vitro to significantly enhance collagen synthesis. A positive effect of stanazolol on wound healing in patients with non-healing wounds has also been demonstrated. Clinical studies show that the treatment with stanozolol during the induction phase of chemotherapy results in a positive effect on the duration of cancer-free remission. each mL contains: Stanozolol USP 50 mg Benzyl Alcohol BP 0.9% v/v Carmellose Sodium BP 0.1% w/v Water for Injections BP q.s.

Sustabol Inject General information: CAS Name: androst-4-en-3-one, 17-[(1-oxoheptyl)-oxy]-, (17?)- androst-4-en-3-one, 17-(3-cyclopentyl-1-oxopropoxy)-, (17?)- 17-(1-Oxopropoxy)-(17b)-androst-4-en-3-one 17b-Hydroxyandrost-4-en-3-one decanoate Sustabol This is a testosterone injection consisting of a mix of propionate, phenylpropionate, isocaproate, and decanoate esters. Because of the mix of different esters, "4 Test Inj" has improved pharmacokinetics with the fast action of propionates and the prolonged action of longer isocaproate and decanoate esters, thus providing a more stable concentration of testosterone in the blood over a longer period of time. Esterification of the 17-beta-hydroxy group by different esters can prolong of action of testosterone, because testosterone esters are less polar than free testosterone. Testosterone esters in oil injected intramuscularly are absorbed slowly from the lipid phase; thus "4 Test Inj" can be given at intervals of two to four weeks. each mL contains: Testosterone Propionate BP 30 mg Testosterone Phenylpropionate 60 mg Testosterone Isocaproate BP 60 mg Testosterone Decanoate BP 100 mg Benzyl Alcohol BP 5.0% v/v Arachis Oil BP q.s.

Testabol Enanthate Inject General information: CAS Name: androst-4-en-3-one, 17-[(1-oxoheptyl)-oxy]-, (17?)- Testabol Testosterone enanthate injection USP, provides testosterone enanthate, a derivative of the primary endogenous androgen testosterone, for intramuscular administration. In their active form, androgens have a 17-beta-hydroxy group. Esterification of the 17-beta-hydroxy group increases the duration of action of testosterone; hydrolysis to free testosterone occurs in vivo. Testosterone esters are less polar than free testosterone. Testosterone esters in oil injected intramuscularly are absorbed slowly from the lipid phase; thus Testosterone Enanthate can be given at intervals of two to four weeks. Testosterone enanthate used in males to treat primary hypogonadism (congenital or acquired) - testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, or orchidectomy. In females: metastatic mammary cancer. Other methods of counteracting estrogen activity in cases of adrenalectomy, hypophysectomy, and/or antiestrogen therapy. each mL contains: Testosterone Enanthate USP 250 mg Benzyl Alcohol BP 3.0% v/v Arachis Oil BP q.s.

Testabol Depot Inject General information: CAS Name: androst-4-en-3-one, 17-(3-cyclopentyl-1-oxopropoxy)-, (17?)- Testabol Testosterone cypionate injection, for intramuscular injection, contains testosterone cypionate which is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone. Testosterone cypionate is used to regulate normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include: growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein. each mL contains: Testosterone Cypionate BP 200 mg Benzyl Alcohol BP 3.0% v/v Arachis Oil BP q.s.

Testabol Propionate Inject General information: CAS Name: 17-(1-Oxopropoxy)-(17b)-androst-4-en-3-one Testabol Testosterone propionate, for intramuscular injection, contains testosterone propionate which is the oil-soluble 4-androstene-3-one,17beta-ol of the androgenic hormone testosterone. Testosterone propoinate is attached to a short ester. Thus, 100mg of testosterone propionate contains 83.72mg of testosterone, more testosterone than in any other ester-based testosterone preparation of equivalent overall dosage. Testosterone propionate is used in males to treat primary hypogonadism (congenital or acquired) - testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome, or orchidectomy. In females: metastatic mammary cancer. Testosterone propionate converts into estrogens and DHT. each mL contains: Testosterone Propionate BP 100 mg Ethyl Oleate BP q.s.

Trenabol Inject General information: CAS Name: 17?-Hydroxyestra-4,9,11-trien-3-one Trenabol Trenbolone acetate (TBA), an androgenic/anabolic steroid (AA), is a potent agonist of androgen receptors and has been extensively used as a growth promoter. TBA is a progestin and does not convert to estrogens. The effects of TBA are increased weight gain, improved food conversion efficiency, decreased muscle RNA and DNA concentrations, and decreased free cathepsin D activity in muscle. The half-life of trenbolone acetate in circulation is one day. each tablet contains: Trenbolone Acetate 80 mg Benzyl Alcohol BP 3.0% v/v Arachis Oil BP q.s.