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Indapamide Structure

PRODUCT TYPE

API

GRADE

BP/USP

CHEMICAL FORMULA

C16H16ClN3O3S

IUPAC NAME

4-Chloro-N-(2-methyl-2,3-dihydro-1H-indol-1-yl)-3-sulfamoylbenzamide

CAS NO

26807-65-8

MOLECULAR WEIGHT

365.83 g/mol

CHEMICAL CLASS

Sulfonamide derivative / Indoline compound

THERAPEUTIC CLASS

Thiazide-like diuretic / Antihypertensive agent

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White to off-white crystalline powder
Solubility Slightly soluble in water; freely soluble in methanol, ethanol, and acetone; practically insoluble in ether and chloroform
Melting Point 160 – 162 °C
pH (1% aqueous solution) 5.0 – 7.0

Product Description

Indapamide is a thiazide-like diuretic (water pill) used primarily to treat high blood pressure (hypertension) and fluid retention (edema) caused by congestive heart failure. Indapamide is known for its excellent bioavailability, long duration of action, and minimal metabolic side effects, making it a preferred choice in modern cardiovascular therapy.

How Indapamide Works

Indapamide acts primarily as a thiazide-like diuretic that reduces blood pressure through a dual mechanism: (1) Renal Action: It inhibits sodium and chloride reabsorption in the distal convoluted tubule of the nephron, leading to increased excretion of sodium, chloride, and water. This mild diuretic effect helps decrease plasma volume and, consequently, lowers cardiac output and blood pressure. (2) Vascular Action: Indapamide also exhibits direct vasodilatory properties by reducing calcium influx into vascular smooth muscle cells, resulting in decreased peripheral vascular resistance. These combined effects lead to a sustained antihypertensive response with minimal metabolic disturbances compared to conventional thiazide diuretics.

Use(s)

Adverse Effects

Why choose Salius for Indapamide?

  1. WHO-GMP Certified Manufacturing
    Salius Pharma produces Indapamide in facilities certified by the World Health Organization’s Good Manufacturing Practices (WHO-GMP), ensuring the API meets high-quality, safety, and purity standards required globally.
  2. Consistent Quality and Reliability
    They maintain strict quality control protocols to provide consistent, pharmaceutical-grade Indapamide. This reliability helps pharmaceutical companies avoid batch failures and regulatory issues.
  3. Global Export Experience & Documentation Support
    Salius regularly exports APIs, provides regulatory documents (DMF, impurity profiles), and supports filings for international clients—even in stringent regulated markets.
  4. Documents We Provide
  5. Focus on Chronic Therapy APIs
    Salius specializes in APIs for chronic diseases, demonstrating expertise in producing reliable compounds like Indapamide, often used in long-term treatments.
Attribute Why Salius Pharma Is a Good Choice
Quality Certification WHO GMP, ISO 9001:2015, FDA audited facilities
Affordability & Generic Access Cost competitive generics for global supply
Export Experience Proven track record of supplying globally

What You Receive in Our Package

When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.

Each Shipment Includes:

Product

Expected Delivery Time

We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.

Overall Delivery Time:

7 to 21 business days from dispatch, depending on your location.

FAQs

Our Indapamide API complies with BP/USP standards and is supported by complete regulatory documentation, including COA, DMF (where applicable), and CTD dossiers. All batches are manufactured under cGMP and ISO-certified facilities.

We export globally with a strong focus on LATAM, MENA, CIS, and Southeast Asia regions. Our products meet the import and registration requirements of multiple regulatory authorities worldwide.

Indapamide is packed in HDPE drums or fiber containers, lined with double polyethylene bags to ensure protection against moisture and contamination. Shipments are handled under standard export conditions — via air or sea freight, depending on client preference and urgency.

Yes. We provide comprehensive regulatory support, including DMF filing assistance, technical data, and product dossiers in CTD format to facilitate product registration in your country.

Our standard MOQ is 25 kg, but we accommodate smaller trial orders for regulatory submissions or formulation development upon request.

Place an Order or Request a Quote from Salius Pharma

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Whether you need Active Pharmaceutical Ingredients (APIs), finished formulations, or regulatory support, our team is ready to provide dependable, compliant, and cost-effective solutions tailored to your market needs.

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