Product Profile

Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup is a comprehensive respiratory formulation combining bronchodilator, expectorant, mucolytic, and soothing actions. As a premier WHO-GMP certified pharmaceutical manufacturer in Baddi, Saar Biotech manufactures this syrup with validated four-API quality control.

Manufacturing Advantage

Why Saar Biotech for Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup?

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 Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup 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 Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup

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

What are the clinical indications for Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup?

This combination syrup is indicated for the symptomatic relief of productive cough associated with bronchospasm, bronchitis, and respiratory infections. Terbutaline provides bronchodilation, Guaiphenesin acts as an expectorant, Bromhexine thins mucus, and Menthol provides soothing relief.

How does this combination work?

Terbutaline is a selective beta-2 agonist that relaxes bronchial smooth muscle, improving airflow. Guaiphenesin increases respiratory secretion volume and reduces mucus adhesiveness. Bromhexine breaks down mucopolysaccharide fibers in mucus, reducing viscosity. Menthol provides a soothing, cooling effect on the respiratory tract.

What is the standard dosing protocol?

The standard adult dose is 5 to 10 ml taken three to four times daily. The syrup should be shaken well before each use and measured with a calibrated dosing device. Treatment duration should be as directed by the physician.

What are the key contraindications and precautions?

This syrup is contraindicated in patients with known hypersensitivity to any component. Terbutaline should be used with caution in patients with cardiovascular disease, hypertension, and hyperthyroidism. Use during pregnancy and lactation should be under physician supervision.

What are the common side effects?

Common side effects may include fine tremors, tachycardia, headache, nausea, and gastrointestinal discomfort. Most of these are mild and transient.
Manufacturing Support

B2B Manufacturing Guide for Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup

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

What pack sizes and packaging options are available for this cough syrup?
Saar Biotech manufactures Terbutaline + Guaiphenesin + Bromhexine + Menthol Syrup in 60 ml and 100 ml bottle formats. Packaging options include: sticker label, metallic label, drip-off brand embossed carton, measuring cap, printed cap, company-logo printed PP cap, with-carton or without-carton supply.
What is the MOQ for this syrup?
Standard MOQ ranges from 5,000 to 10,000 units per SKU, depending on bottle size, label type, and carton format.
What analytical tests are performed on every manufacturing batch?
Every batch undergoes HPLC Assay confirming all four actives, pH and viscosity testing, and Microbial Limit Testing (MLT). A Certificate of Analysis (COA) is issued.
What is the turnaround time for a new order?
Initial third-party production typically requires 30 to 45 working days following packaging confirmation. Repeat orders are fulfilled in 20–25 working days.
Do you offer private labelling and packaging design?
Yes, our in-house design team provides end-to-end support for private label packaging, including mono-cartons, labels, and promotional materials compliant with regulatory guidelines.
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