Active Pharmaceutical Ingredients
Sildenafil Citrate DC Granules are ready-to-compress pharmaceutical intermediates designed for the direct compression of erectile dysfunction (ED) tablets. These granules are pre-formulated with functional excipients to ensure excellent flowability, compressibility, and content uniformity, making them highly suitable for efficient, high-speed tablet manufacturing. The formulation enables the rapid onset of action, with Sildenafil Citrate acting as a selective phosphodiesterase type 5 (PDE5) inhibitor to improve blood flow and support the treatment of ED and related vascular conditions.
| Component | Function |
|---|---|
| Sildenafil Citrate | Active Pharmaceutical Ingredient (API) – PDE5 inhibitor for erectile dysfunction and vasodilation |
| Pregelatinized Starch / Starch 1500 | Binder & Disintegrant – Provides granule cohesion and ensures rapid disintegration |
| Colloidal Silicon Dioxide | Glidant – Improves powder flowability and prevents clumping during tablet compression |
| Magnesium Stearate | Lubricant – Reduces friction and prevents sticking to punches and dies during tableting |
| Purified Water | Granulating Solvent – Used during wet granulation; evaporates during the drying process |
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.
We ensure prompt and reliable shipping worldwide. Delivery times may vary depending on destination, order volume, and regulatory requirements.
Looking to source Sildenafil Citrate 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.
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Any patented products are excluded from our offerings in regions where such patents are currently in force.
24–36 months, depending on packaging and storage conditions.
Yes, compatible with standard tableting excipients such as MCC, lactose, dicalcium phosphate, and lubricants..
Yes, they can meet USP, BP, EP, or IP specifications, depending on customer and market requirements.