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Product Overview

Duloxetine SR (Sustained Release) Pellets are formulated to provide a controlled release of duloxetine hydrochloride, a serotonin-norepinephrine reuptake inhibitor (SNRI). They are primarily used in the treatment of major depressive disorder, generalized anxiety disorder, neuropathic pain, fibromyalgia, and chronic musculoskeletal pain. The SR formulation ensures prolonged therapeutic activity, reducing dosing frequency and improving patient compliance.

Acetaminophen DC Granules – Typical Composition

Component Function
Duloxetine Hydrochloride Active Pharmaceutical Ingredient (API)
Sugar Spheres / MCC Spheres Inert core or starter pellets
Hydroxypropyl Methylcellulose (HPMC) Binder / Film former during layering
Talc / Colloidal Silicon Dioxide Anti-adherent / Glidant
Ethylcellulose / Eudragit RS/RL Sustained release polymer (controls drug release)
Triethyl Citrate / PEG 6000 Plasticizer (for polymer coating)
Purified Water Solvent (removed after processing)

Why Choose Pellets from Salius Pharma?

Outsourcing pellets through a trusted partner like Salius Pharma can be a strategic decision to save both time and resources, without compromising 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 Duloxetine SR Pellets 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.

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

FAQs

They are used in the treatment of depression, anxiety, neuropathic pain, and fibromyalgia.

Absolutely. They can be combined with other pellet types (e.g., immediate release or delayed release) in multi-unit pellet system (MUPS) capsules or tablets.

They comply with pharmacopeial guidelines (USP/EP/BP) and must meet ICH stability and cGMP manufacturing requirements.

We provide COA (Certificate of Analysis), MSDS (Material Safety Data Sheet), Stability Data, and necessary regulatory support documents.

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