Products

Drug Name: Dutasteride Strength: 0.5 mg per capsule/tablet Dosage Form: Soft gelatin capsule (most common) Oral administration Mechanism of Action: Inhibits both type I and type II 5-alpha-reductase enzymes, reducing the conversion of testosterone to dihydrotestosterone (DHT). Lower DHT levels lead to prostate shrinkage and improvement in urinary symptoms. Dutasteride is a medication primarily used to treat an enlarged prostate (benign prostatic hyperplasia, BPH) in men. It works by blocking the conversion of testosterone to dihydrotestosterone (DHT), a hormone that can cause the prostate to grow. 1.Benign Prostatic Hyperplasia (BPH): Helps reduce prostate size. Improves urinary symptoms like difficulty urinating, weak stream, and frequent urination. 2.Prevention of urinary retention and the need for prostate surgery in men with enlarged prostate.

Mytret C Gel is a prescription dermatological medication used to treat various skin conditions, primarily acne. It is classified as a combination topical antibiotic and retinoid preparation. Application: It is typically applied in a thin layer to clean, dry, affected skin, usually at bedtime. Sunlight Sensitivity: The tretinoin in the gel increases your skin's sensitivity to sunlight, so it's important to use sun protective measures (sunscreen, protective clothing) when outdoors. Acne Vulgaris: This is its primary use, helping to manage mild to moderate acne, including pimples, blackheads, and whiteheads. Oily Skin: The gel helps control excessive oil production, which prevents pores from becoming clogged. Skin Inflammation: It can help manage the mild inflammation and redness associated with acne breakouts. Sun-Damaged Skin: By stimulating cell turnover, it can help revive sun-damaged skin, and may help reduce fine lines and wrinkles. Hyperpigmentation: It can help improve uneven skin tone, dark spots, and patchy discoloration. Mytret gel is a skincare solution utilised for addressing various skin conditions, particularly those characterised by excessive oil production. Being a form of vitamin A, the primary function of this gel revolves around its capacity to regulate oil secretion in the skin. By doing so, it assists in unclogging and loosening pores on the skin's surface, addressing potential problems that may arise if left untreated. The effectiveness of Mytret 0.04 gel is particularly notable in its ability to combat common skin problems such as pimples, whiteheads, and blackheads. These issues commonly stem from blocked pores, a challenge that this gel actively tackles. Consistent use of Mytret gel can notably diminish these concerns by promoting the maintenance of clear pores and regulating oil secretion. Essentially, Mytret 0.04 gel offers an efficient solution for addressing specific skin conditions, providing substantial relief from problems associated with blocked pores and excessive oil production. Active Ingredients Clindamycin (an antibiotic) and Tretinoin (a form of Vitamin A/retinoid)

Generic Name : Trestolone Trestolone (7α-methyl-19-nortestosterone) is a synthetic androgen developed by the Population Council as a potential candidate drug for use in hormonal male contraceptive methods. In males, regular administration of sufficient quantities of trestolone induces a state of temporary infertility. Trestolone acetate (also called 7α-methyl-19-nortestosterone, MENT acetate) is a synthetic anabolic–androgenic steroid (AAS). Male contraception Investigational use as a potent androgen that suppresses spermatogenesis while maintaining secondary sex characteristics. Hypogonadism in men (experimental) Explored as a long-acting androgen therapy for low testosterone. Key properties Highly androgenic and anabolic Does not aromatize to estrogen Potent at low doses due to strong receptor affinity Long-lasting effects in injectable form Rapid muscle mass gain: It has a highly favorable anabolic-to-androgenic ratio, making it effective for building muscle. Increased strength: It is considered extremely powerful, surpassing the strength of natural testosterone, leading to significant strength enhancement.

Tamoxifen API (Active Pharmaceutical Ingredient) is the pure, bulk powder form of the drug Tamoxifen Citrate, a key selective estrogen receptor modulator (SERM) used mainly to treat and prevent hormone-receptor-positive breast cancers, working as an anti-estrogen by blocking estrogen's effects on cancer cells. INN / Common name: Tamoxifen citrate CAS No.: 54965-24-1 Molecular formula: C₂₈H₃₂N₂O·C₆H₈O₇ (citrate salt) Molecular weight: ~563.64 g/mol Breast cancer treatment For estrogen receptor–positive (ER+) breast cancer in pre- and postmenopausal women. Used in adjuvant therapy (after surgery) or treatment of metastatic disease. Breast cancer prevention In high-risk women, tamoxifen reduces the risk of developing breast cancer. Other estrogen-related conditions (off-label, limited) Certain gynecomastia cases in men Fertility treatments (rare off-label use in women to induce ovulation) Mechanism of action (brief) Tamoxifen blocks estrogen receptors in breast tissue, preventing estrogen from promoting tumor growth. In other tissues (bone, uterus), it may act as a partial agonist, producing estrogen-like effects. Identification IR spectroscopy: Conforms to reference spectrum UV / HPLC: Retention time matches certified reference standard Melting point: Within reference range (~140–144 °C for citrate salt) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

Clomifene Citrate Raw API (Active Pharmaceutical Ingredient) is the pure, bulk powder form of the drug used in manufacturing fertility medicines, primarily to induce ovulation in women with ovulation issues like PCOS, working as a SERM (Selective Estrogen Receptor Modulator) by stimulating hormone release for egg growth. Usage: An essential ingredient in making ovulation-inducing medications INN / Common name: Clomifene citrate CAS No.: 50-41-9 Molecular formula: C₂₆H₂₈ClNO·C₆H₈O₇ (citrate salt) Molecular weight: ~598.08 g/mol Identification IR spectroscopy: Conforms to reference spectrum UV / HPLC: Retention time matches certified reference standard Melting point: Within reference range (~109–110 °C for citrate salt) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

INN / Common name: Stanolone / Dihydrotestosterone (DHT) CAS No.: 521-18-6 Molecular formula: C₁₉H₃₀O₂ Molecular weight: ~290.45 g/mol Identification IR spectroscopy: Conforms to reference spectrum HPLC / UV: Retention time matches certified reference standard Melting point: Within reference range (~180–184 °C) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis) Androgen Deficiency and Male Hypogonadism: Stanolone is primarily used as a hormone replacement therapy for men with low testosterone levels or other forms of androgen deficiency. Treatment of Specific Conditions in Males: It can be used to treat certain conditions related to androgen development, such as microphallus (small penis) in infancy or males, and male breast development. Muscle Wasting Diseases and Osteoporosis: Due to its potent anabolic properties, it has been explored for treating muscle wasting diseases and osteoporosis, promoting muscle growth and maintaining bone density. Aplastic Anemia: It may be used in the treatment of rare forms of aplastic anemia that are responsive to anabolic androgens.

The Exemestane Raw Active Pharmaceutical Ingredient (API) is primarily used for manufacturing medications to treat hormone-receptor-positive breast cancer in postmenopausal women. INN: Exemestane CAS No.: 107868-30-4 Molecular formula: C₂₀H₂₄O₂ Molecular weight: ~296.41 g/mol White to off-white crystalline powder Practically insoluble in water; soluble in organic solvents Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

Muscle Growth: Promotes protein synthesis, leading to significant increases in muscle size and mass. Strength Enhancement: Known for producing rapid and substantial strength gains. Athletic Performance: Used to enhance overall performance in strength sports and weight training. Fat Loss: Some users report concurrent fat reduction, possibly due to an increased metabolic rate from added muscle mass. Specifications : INN / Common name: Methasterone Other name: Superdrol CAS No.: 3381-88-2 Molecular formula: C₂₁H₃₄O₂ Molecular weight: ~318.49 g/mol Assay (Potency) Commonly 98.0% – 102.0% (on anhydrous basis), per internal specification

Generic Name : Mesterolone Mesterolone is a synthetic anabolic-androgenic steroid (AAS) and derivative of dihydrotestosterone (DHT). It is inactivated by 3α-hydroxysteroid dehydrogenase in skeleta muscules so it is considered a weak androgen. It is not a substrate for aromatase so it is not converted into estrogen. Mesterolone demonstrated to have minimal effect on sperm counts and levels of FSH or LH 1,2. Experiments of mesterolone serving as a potential treatment of depression are still undergoing. Male Hypogonadism/Androgen Deficiency: The primary medical use is to treat low testosterone levels in men due to hypogonadism (a condition where the testes produce little or no hormones). This helps restore normal sexual function, mood, and energy levels. Male Infertility: It is used to manage male infertility that stems from low androgen levels, as it can improve sperm count and quality in affected men. INN: Mesterolone CAS No.: 1424-00-6 Molecular formula: C₂₀H₃₂O₂ Molecular weight: ~304.47 g/mol Assay (Potency) Typically 98.0% – 102.0% (on anhydrous basis), depending on pharmacopeial or internal standard

“Turinabol raw API“ refers to the raw active pharmaceutical ingredient (API) of 4-chlorodehydromethyltestosterone (CDMT), an anabolic steroid. Its primary use is in performance enhancement, specifically for muscle growth and athletic performance. INN / Common name: Chlorodehydromethyltestosterone (Turinabol) CAS No.: 2446-23-3 Molecular formula: C₂₀H₂₇ClO₂ Molecular weight: ~334.88 g/mol Performance Enhancement: Turinabol is widely used by athletes and bodybuilders to increase lean muscle mass and strength without significant water retention or estrogenic side effects (like gynecomastia or bloating). Aesthetic Conditioning: Due to its “dry“ gains and ability to preserve muscle during caloric deficits, it is popular during “cutting“ cycles for aesthetic purposes or for athletes in weight-restricted sports. Increased Endurance and Recovery: It enhances nitrogen retention and red blood cell production, which improves oxygen delivery to muscles and aids in faster post-training recovery. Identification IR spectroscopy: Conforms to reference spectrum HPLC/UV: Retention time matches certified reference standard Assay (Potency) Typically 98.0% – 102.0% (on anhydrous basis), depending on standard applied

Oxymetholone raw active pharmaceutical ingredient (API) is used to produce medications for various medical conditions, primarily anemias and muscle-wasting syndromes, as well as for illicit performance enhancement in sports. INN: Oxymetholone CAS No.: 434-07-1 Molecular formula: C₂₁H₃₂O₃ Molecular weight: ~332.48 g/mol White to off-white crystalline powder Practically insoluble in water; soluble in certain organic solvents USES : Bodybuilding, muscle enhancement, or performance enhancement Cosmetic or recreational use Oxymetholone binds to androgen receptors inside target cells (e.g., bone marrow, muscle). The drug–receptor complex moves into the cell nucleus. There, it binds to specific DNA sequences (androgen response elements), changing gene expression.

Metandienone (also known as Methandrostenolone or Dianabol) is a synthetic anabolic–androgenic steroid (AAS) derived from testosterone. Metandienone (Dianabol) — API Specification Name: Metandienone Synonyms: Methandrostenolone, Dianabol Chemical class: Anabolic–androgenic steroid (AAS) CAS Number: 72-63-9 Molecular Formula: C₂₀H₂₈O₂ Molecular Weight: ~300.44 g/mol Description: 17-alpha-alkylated anabolic steroid API Assay / Purity Typical pharmaceutical API quality expectations: Assay (potency): 97.0% – 103.0% Related substances / impurities: Within specified limits Residual solvents: Compliant with ICH Q3C guidelines Heavy metals: Within pharmacopeial limits Metandienone enters androgen-responsive cells (e.g., skeletal muscle) It binds to the androgen receptor (AR) in the cytoplasm The hormone–receptor complex translocates into the cell nucleus It binds to androgen response elements (AREs) on DNA USES : Muscle wasting conditions Severe weight loss Osteoporosis Recovery from major illness or surgery