+91 84258 80640 export@saliuspharma.com

Product Overview

Olmesartan DC Granules are ready-to-compress pharmaceutical intermediates designed for the direct compression of Olmesartan tablets. These granules are pre-formulated with functional excipients to ensure excellent flowability, compressibility, and content uniformity, making them ideal for efficient and high-speed tablet manufacturing processes.

Olmesartan DC Granules

Olmesartan DC Granules – Typical Composition

Component Function
Olmesartan Active Pharmaceutical Ingredient (API)
Pregelatinized Starch / Starch 1500 Binder & Disintegrant
Colloidal Silicon Dioxide Glidant
Magnesium Stearate Lubricant
Purified Water Granulating Solvent

Why Choose Granules from Salius Pharma?

Outsourcing DC Granules through a trusted partner like Salius Pharma can be a strategic decision to save both time and resources, without compromise on quality or compliance.
Instead, partnering with Salius Pharma—a leading distributor aligned with USFDA-approved and WHO-GMP-certified manufacturers in India—allows you to leverage high-quality products, seamless logistics, and professional support under one roof.

Key Advantages of Partnering with Salius Pharma

Expected Delivery Time

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

Place an Order or Request a Quote from Salius Pharma

Looking to source Olmesartan DC Granules or other high-quality pharmaceutical pellet formulations?
Whether you need Active Pharmaceutical Ingredients (APIs), excipients, or regulatory support, our team is ready to provide reliable, compliant, and cost-effective solutions tailored to your market needs.

Get in Touch

Confidentiality Notice

The contents of this page and any attachments are intended solely for the designated recipient(s) and may contain confidential and/or privileged information protected by law.

Any patented products are excluded from our offerings in regions where such patents are currently in force.

FAQs

Yes, they are manufactured under GMP conditions and can be supplied in compliance with USP, EP, BP, or IP specifications as per market requirements.

Documentation includes Certificate of Analysis (CoA), MSDS, GMP certificate, manufacturing license, stability data, and technical data sheets upon request.

The standard shelf life ranges from 24 to 36 months, depending on packaging configuration and stability data.

Send Enquiry
Chat With Us!
Call Us!
Mail Us!