Product Profile

Magaldrate + Simethicone Suspension is a clinically established, non-systemic antacid and anti-flatulent formulation indicated for hyperacidity, heartburn, and gas-related discomfort. As a premier WHO-GMP certified pharmaceutical manufacturer in Baddi, Saar Biotech manufactures this suspension with validated two-API quality control and precise rheological control, ensuring reliable antacid performance in every 5ml dose.

Manufacturing Advantage

Why Saar Biotech for Magaldrate + Simethicone Suspension?

Since {{ site.Params.founded }}, Saar Biotech has been a distinguished WHO-GMP certified leader in pharmaceutical manufacturing. We utilize advanced micronization and pH-stabilization protocols to deliver unmatched bioavailability for this Magaldrate + Simethicone Suspension formulation.

DCGI Approved

Comprehensive documentation and CDSCO support for rapid market entry in India.

Fast Turnaround

30-45 days lead time for new batches with state-of-the-art logistics.

Pan-India Supply & Contract Manufacturing

Batch Lead Time 30-45 Days (Domestic)
B2B Services Contract & Third-Party
Compliance DCGI & Schedule M Standards
Medical Intelligence

Clinical Q&A for Magaldrate + Simethicone Suspension

Technical data on bioavailability, pediatric dosing protocols, and therapeutic efficacy for healthcare professionals.

What are the clinical indications for Magaldrate + Simethicone Suspension?

This combination suspension is indicated for the symptomatic relief of hyperacidity, heartburn, acid indigestion, gastritis, and flatulence. Magaldrate provides rapid and sustained acid neutralisation without causing systemic alkalosis, while Simethicone reduces gas bubbles in the gastrointestinal tract, providing relief from bloating and discomfort. The combination is effective for both acute and chronic acid-related gastrointestinal conditions.

How does Magaldrate differ from other antacids?

Magaldrate is a unique hydroxy-magnesium aluminate with a high acid-neutralising capacity. Unlike simple aluminium or magnesium hydroxide combinations, Magaldrate provides rapid acid neutralisation with sustained action. Its non-systemic nature means it is not significantly absorbed, reducing the risk of systemic side effects such as alkalosis or electrolyte imbalance commonly associated with sodium-containing antacids.

What is the standard dosing protocol?

The standard adult dose is 5 to 10 ml taken 3 to 4 times daily, 20 minutes to 1 hour after meals and at bedtime, or as directed by a physician. The suspension should be shaken well before each use. The dose should be taken undiluted for maximum effectiveness. Treatment duration should be as prescribed by the physician.

What are the key contraindications and precautions?

This suspension is contraindicated in patients with known hypersensitivity to any component. Caution is advised in patients with renal impairment, as magnesium accumulation may occur. It should be used with caution in patients on sodium-restricted diets and those with gastrointestinal obstruction. Use during pregnancy and lactation should be under physician supervision.

What drug interactions should be considered?

This antacid should be taken at least 2 hours apart from other medications, as it may interfere with the absorption of drugs such as tetracyclines, fluoroquinolones, iron supplements, and levothyroxine. Patients should be counselled to maintain appropriate dosing intervals between this suspension and other oral medications.
Manufacturing Support

B2B Manufacturing Guide for Magaldrate + Simethicone Suspension

Detailed insights on MOQs, lead times, and regulatory support for contractmanufacturing partners.

What pack sizes and packaging options are available for Magaldrate Suspension?
Saar Biotech manufactures Magaldrate + Simethicone Suspension in 170 ml bottle formats. The 170 ml pack is the primary commercial format for antacid suspensions. Packaging options include: sticker label, metallic label, measuring cap, bell cap, printed cap, company-logo printed PP cap, with-carton or without-carton supply, and sleeve pack options. Shipper configurations of 64×170ml support distributor-level bulk dispatch.
What is the MOQ for Magaldrate + Simethicone Suspension?
Standard MOQ ranges from 5,000 to 10,000 units per SKU, depending on bottle size, label type, and carton format. Antacids are among the highest-velocity consumer healthcare products in India with consistent year-round demand.
What analytical tests are performed on every manufacturing batch?
Every batch undergoes titrimetric Assay for Magaldrate and Simethicone content verification against IP specifications. Suspension uniformity and re-dispersibility testing ensures dose consistency. pH and viscosity testing confirms suspension stability. Microbial Limit Testing (MLT) meets IP specifications. A Certificate of Analysis (COA) is issued with every B2B consignment.
Does Saar Biotech support brand name registration and DCGI approval?
Yes. Our regulatory team provides end-to-end support for DCGI brand name search and approval for antacid products. We assist partners in verifying that their chosen brand name is available and compliant with DCGI nomenclature guidelines.
What is the turnaround time for a new Magaldrate Suspension order?
Initial third-party production typically requires 30 to 45 working days following packaging confirmation. Consistent repeat commercial orders are swiftly handled within a 20 to 25 working day window.
What is the turnaround time for a new Magaldrate + Simethicone Suspension order?
New third-party antacid suspension orders are dispatched from our oral suspension facility in Baddi within 30 to 45 working days of packaging artwork finalisation. For established gastroenterology brands placing repeat orders, our high-throughput liquid filling lines ensure batch completion within 20 to 25 working days, supporting consistent shelf availability.
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