Product Profile

Deflazacort 6mg Oral Suspension is a clinically established corticosteroid formulation indicated for the management of inflammatory and immunological conditions. As a premier WHO-GMP certified pharmaceutical manufacturer in Baddi, Saar Biotech manufactures this suspension with validated API quality control, ensuring reliable therapeutic performance in every 5ml dose.

Manufacturing Advantage

Why Saar Biotech for Deflazacort Oral 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 Deflazacort Oral 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 Deflazacort Oral Suspension

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

What are the clinical indications for Deflazacort 6mg Suspension?

Deflazacort is indicated for the management of inflammatory and immunological conditions including rheumatoid arthritis, asthma, allergic conditions, and skin disorders. It is also used in Duchenne muscular dystrophy. As a corticosteroid, it reduces inflammation by suppressing the immune response.

What makes Deflazacort different from other corticosteroids?

Deflazacort is an oxazoline derivative of prednisolone. It has been shown to have a lower incidence of certain side effects compared to other corticosteroids, particularly less impact on bone metabolism. The suspension form allows for accurate, flexible dosing in pediatric and elderly patients.

What is the standard dosing protocol?

Dosing should be individualised and directed by a physician. The suspension should be shaken well before each use. A calibrated measuring device should be used for accurate dosing. Treatment should be at the lowest effective dose for the shortest duration.

What are the key contraindications and precautions?

Deflazacort is contraindicated in patients with systemic fungal infections and known hypersensitivity. Caution is advised in patients with diabetes, hypertension, osteoporosis, glaucoma, and gastrointestinal disorders. Use during pregnancy and lactation requires physician supervision.

What are the common side effects?

Common side effects may include increased appetite, weight gain, mood changes, insomnia, and gastrointestinal discomfort. Prolonged use may lead to osteoporosis, adrenal suppression, and other corticosteroid-related effects.
Manufacturing Support

B2B Manufacturing Guide for Deflazacort Oral Suspension

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

What pack sizes and packaging options are available for Deflazacort Suspension?
Saar Biotech manufactures Deflazacort 6mg Suspension in 30 ml and 60 ml bottle formats. Packaging options include: sticker label, drip-off brand embossed carton, measuring cap, printed cap, with-carton or without-carton supply.
What is the MOQ for this suspension?
Standard MOQ ranges from 5,000 to 10,000 units per SKU, depending on bottle size and packaging specification.
What analytical tests are performed on every batch?
Every batch undergoes HPLC Assay confirming Deflazacort content, suspension uniformity testing, pH and viscosity testing, and Microbial Limit Testing (MLT). A Certificate of Analysis (COA) is issued with every B2B consignment.
Does Saar Biotech assist with brand name registration and DCGI approval for Deflazacort?
Yes. Our regulatory team provides end-to-end support for DCGI brand name search and registration specifically for corticosteroid products. We guide clients through the Schedule H product classification requirements and ensure all labelling meets DCGI-mandated corticosteroid warnings and Storage Schedule M specifications for liquid formulations.
What is the turnaround time for a new Deflazacort Suspension order?
Initial third-party production typically requires 30 to 45 working days following packaging artwork confirmation and licensing clearance. For established partners with repeat corticosteroid suspension orders, our liquid manufacturing lines in Baddi typically fulfil batches within 20 to 25 working days.
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