Hydrochlorothiazide USP is a pharmaceutical-grade thiazide diuretic recognized for its FDA-approved efficacy in managing hypertension and peripheral edema. It functions by inhibiting sodium resorption in the distal convoluted tubules of the kidneys, leading to increased excretion of sodium and water, thereby reducing blood volume and blood pressure. This makes Hydrochlorothiazide USP an essential medication for healthcare providers in treating patients with high blood pressure and fluid retention conditions. Its USP (United States Pharmacopeia) designation ensures that the product meets strict quality, purity, and potency standards required for medical use, making it a reliable choice for pharmaceutical manufacturers and healthcare institutions in the B2B sector.
Key Features
| Features | Description |
|---|---|
| Active Ingredient | Hydrochlorothiazide USP |
| Therapeutic Use | Treatment of Hypertension and Peripheral Edema |
| Mechanism of Action | Inhibits sodium resorption in distal convoluted tubules of kidneys |
| Dosage Form | Pharmaceutical-grade powder or granules for formulation |
| Regulatory Approval | FDA Approved |
| Standard Compliance | Meets United States Pharmacopeia (USP) quality standards |
| Pharmacological Class | Thiazide diuretic |
| Effect | Increases sodium and water excretion, reducing blood volume |
| Intended Use | For pharmaceutical manufacture and hospital use |
| Attributes | Description |
|---|---|
| Chemical Name | Hydrochlorothiazide |
| CAS Number | 58-93-5 |
| Molecular Formula | C7H8ClN3O4S2 |
| Molecular Weight | 297.74 g/mol |
| Purity | >= 98% (USP grade) |
| Appearance | White to off-white crystalline powder |
| Solubility | Sparingly soluble in water, freely soluble in sodium hydroxide solution |
| Storage Condition | Store in a cool, dry place, protected from light |
| Packaging | Available in pharmaceutical-grade sealed containers |
*Disclaimer: The above description has been AI-generated and has not been audited or verified for accuracy. It is recommended to verify product details independently before making any purchasing decisions.
Yes, this Hydrochlorothiazide meets USP standards, making it suitable for formulation into pharmaceutical products.
The product maintains a purity of 98% or higher, adhering to USP grade requirements.
Yes, it is intended for use by pharmaceutical manufacturers and hospitals for compounding medications.
Store in a cool, dry place, protected from light, to maintain stability and potency.
Yes, the Hydrochlorothiazide USP supplied is compliant with Indian regulatory standards suitable for pharmaceutical API listing.
