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Mebeverine HCl Structure

Product Type

API

Grade

BP/EP

Chemical Formula

C25H36ClNO5

IUPAC Name

4-(ethyl(p-methoxy-alpha-methylphenethyl)amino)butyl ester, hydrochloride

CAS Number

2753-45-9

Molecular Weight

466.07 g/mol

Chemical Class

Mebeverine

Therapeutic Class

Anti-Spasmodic

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White to off-white crystalline powder
Solubility Slightly soluble in water; soluble in alcohol and chloroform
Melting Point 140–145°C
pH 5–6

Product Description

Mebeverine HCl is an antispasmodic medication used to relieve muscle spasms in the gastrointestinal tract. It works by directly relaxing the smooth muscles of the gut without affecting normal bowel movements. This makes it effective in treating symptoms of irritable bowel syndrome (IBS), including abdominal pain, cramping, and discomfort. Mebeverine helps improve gut motility and reduces spasms, offering symptomatic relief without causing sedation or affecting the central nervous system. It is commonly prescribed worldwide under various brand names and is generally well-tolerated with a low incidence of side effects.

How Mebeverine HCl Works

Mebeverine Hydrochloride works by directly relaxing the smooth muscles of the gastrointestinal tract. It acts as a musculotropic antispasmodic, reducing muscle spasms and cramps without affecting normal gut motility or causing sedation. This helps relieve abdominal pain and discomfort associated with conditions like irritable bowel syndrome (IBS).

Use(s)

Adverse Effects

Why choose Salius for Mebeverine HCl?

  1. WHO-GMP Certified Manufacturing
    Salius Pharma produces Mebeverine HCl 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 Mebeverine HCl. 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 Mebeverine HCl, 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

It is used to relieve abdominal pain and muscle spasms in conditions like irritable bowel syndrome (IBS).

Usually taken as a 135 mg tablet three times daily, preferably 20 minutes before meals, or as prescribed by your doctor.

Relief can be noticed within a few days, but full benefit may take 1–2 weeks.

Yes, Salius Pharma Pvt. Ltd. exports Mebeverine Hydrochloride (HCl) API to various international markets, including countries in Africa and the Middle East. As a Government of India-recognized Star Export House, Salius Pharma has a strong global presence and supplies a wide range of pharmaceutical raw materials to these regions.

Yes, Salius Pharma Pvt. Ltd. provides comprehensive technical support and regulatory documentation for Mebeverine Hydrochloride (HCl) API. Their Regulatory Affairs team offers essential documents such as Drug Master Files (DMF), Certificate of Suitability (CEP), clinical trial data, bioequivalence/bioavailability studies, impurity profiles, and technical dossiers prepared according to international guidelines like ACTD and CTD. This ensures smooth and efficient regulatory submissions for their clients worldwide. For more information or to request documentation, customers can contact Salius Pharma directly via email, phone, or their official website.

Place an Order or Request a Quote from Salius Pharma

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