Granules List
| SN | Product Name | Type | Indication/Therapeutic Class | BCS Class |
|---|---|---|---|---|
| 1 | Asprin granules 500mg and 1000mg | Granules | Pain relief (analgesic), fever (antipyretic), and anti-inflammatory | Class B |
| 2 | Mesalazine granules 1000mg and 2000mg | Granules | Induction and maintenance of remission in mild to moderate ulcerative colitis | Class A |
Frequently Asked Questions
Pharmaceutical granules are agglomerates of powder particles formed through a granulation process, typically ranging from 0.2 to 4.0 mm in size. Unlike fine powders, granules offer better flow properties, reduced dust, and improved content uniformity. Compared to tablets, granules offer faster disintegration and are easier to swallow, making them ideal for pediatric, geriatric, and patients with swallowing difficulties.
Pharmgenity Health manufactures pharmaceutical granules including Aspirin granules (500mg and 1000mg) for analgesic, antipyretic, and anti-inflammatory use, and Mesalazine granules (1000mg and 2000mg) for induction and maintenance of remission in mild to moderate ulcerative colitis. We also offer customized granule formulations for various therapeutic segments.
Granules offer several advantages for export markets: they allow flexible dosing (sachet-based), have better stability than liquid formulations, are lighter and more cost-effective for shipping, and have longer shelf life. Granules also enable combination therapies in a single sachet and are particularly preferred in markets with high demand for pediatric and geriatric-friendly dosage forms.
Yes, we offer customized granule formulations including immediate release, delayed release, and sustained release profiles tailored to specific therapeutic requirements. We can develop granules with taste-masking for improved palatability, and specific particle size distribution for optimal performance. Packaging options include sachets, stick packs, and bulk packaging with custom branding.
Our granules are manufactured in WHO-GMP certified facilities and comply with USP, BP, IP, and EP pharmacopeial standards. Each batch undergoes rigorous testing for particle size distribution, flow properties, drug content uniformity, dissolution profile, moisture content, and microbial limits. Stability studies are conducted as per ICH guidelines to ensure product integrity throughout the shelf life.