PHARMAX LIFESCIENCES

Feature

• Citalopram IP/BP/USP Powder is a pharmaceutical-grade raw material used in the formulation of medications for the treatment of depression and anxiety disorders. It is classified as a selective serotonin reuptake inhibitor (SSRI), working by increasing serotonin levels in the brain to help improve mood, emotional stability, and overall mental health. This high-purity powder complies with IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards, ensuring quality, safety, and consistency for pharmaceutical manufacturing. Intended strictly for research, formulation, or industrial use under professional supervision. Not for direct human consumption without proper formulation and medical direction.

• Powder is a pharmaceutical-grade raw material used in the formulation of medications for the treatment of depression and anxiety disorders. It is classified as a selective serotonin reuptake inhibitor (SSRI), working by increasing serotonin levels in the brain to help improve mood, emotional stability, and overall mental health. This high-purity powder complies with IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards, ensuring quality, safety, and consistency for pharmaceutical manufacturing. Intended strictly for research, formulation, or industrial use under professional supervision. Not for direct human consumption without proper formulation and medical direction.

Feature

Fenofibrate IP/BP/USP Powder – 100 Words Feature

Fenofibrate is a lipid-lowering agent used primarily to treat hypercholesterolemia and hypertriglyceridemia. This white to off-white crystalline powder meets IP, BP, and USP specifications, ensuring pharmaceutical-grade purity and consistency. It acts by activating peroxisome proliferator-activated receptor alpha (PPARα), which increases lipolysis and elimination of triglyceride-rich particles. Fenofibrate effectively reduces LDL cholesterol and triglycerides while increasing HDL cholesterol. It is practically insoluble in water but soluble in organic solvents like methanol and acetone. The powder form is ideal for tablet and capsule formulations. It remains stable under dry, cool storage conditions, making it suitable for long-term pharmaceutical use and formulation development.

Features
Hydrochlorothiazide IP/BP/USP Powder – 100 Words Feature

Hydrochlorothiazide is a thiazide diuretic widely used in the treatment of hypertension and edema associated with heart failure, liver cirrhosis, and renal disorders. Supplied as a fine, white to off-white crystalline powder, it conforms to IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards, ensuring high-quality pharmaceutical-grade purity. The compound functions by inhibiting sodium and chloride reabsorption in the distal renal tubules, promoting diuresis and reducing blood volume. It is odorless, practically insoluble in water, but soluble in acetone and dilute ammonia. Ideal for formulation in tablets and combination therapies, it is stable under recommended storage conditions.

Feature

• Citalopram IP/BP/USP Powder is a pharmaceutical-grade raw material used in the formulation of medications for the treatment of depression and anxiety disorders. It is classified as a selective serotonin reuptake inhibitor (SSRI), working by increasing serotonin levels in the brain to help improve mood, emotional stability, and overall mental health. This high-purity powder complies with IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards, ensuring quality, safety, and consistency for pharmaceutical manufacturing. Intended strictly for research, formulation, or industrial use under professional supervision. Not for direct human consumption without proper formulation and medical direction.