Leading Manufacturers, Exporters, Wholesaler and Retailer of Crodis XL 10 a Crospovidone, Crodis XL 10 B Crospovidone, Lactisol Lactose Monohydrate, Mabitab 1500 Partially Pregelatinized Starch, Mabitab 3000 Fully Pregelatinized Starch, Povimine K30 Povidone Powder, Maltosure Maltodextrin, Povimine K90 Povidone Powder, Mapectin Pectin, Stearex Calcium Stearate Powder, Mylcel Low Substituted Hydroxypropyl Cellulose and Stearion Magnesium Stearate Powder from Pune.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Free-flowing Powder |
| Particle Size (D50) | ~110 µm (Type A, Coarser) |
| Loss On Drying | ≤ 5.0% |
| PH (1% Suspension) | 5.0 – 8.0 |
| Peroxide Value | ≤ 400 Ppm |
| Nitrogen Content | 11.0 – 12.8% |
| Wicking Rate | Rapid |
| Swelling Capacity | High (no Gel Formation) |
CRODIS XL-10 A is a WHO-GMP certified Crospovidone Type A (crosslinked polyvinylpyrrolidone) manufactured in Pune, India. With high wicking and swelling capacity and coarser particle size (~110 µm), it is designed as a super-disintegrant in orally disintegrating tablets (ODT), immediate-release tablets, and fast-dissolving dosage forms. Its insoluble crosslinked structure ensures rapid water uptake without gel formation, achieving disintegration in under 30 seconds in ODTs. Meets USP/NF, EP, and IP. Exported from India to 50+ countries with full pharmacopoeial documentation.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Fine Powder |
| Particle Size (D50) | ~30 µm (Type B, Finer) |
| Loss On Drying | ≤ 5.0% |
| PH (1% Suspension) | 5.0 – 8.0 |
| Peroxide Value | ≤ 400 Ppm |
| Nitrogen Content | 11.0 – 12.8% |
| Wicking Rate | Very Rapid |
| Bulk Density | ~0.3 G/mL |
CRODIS XL-10 B is a WHO-GMP certified fine-particle Crospovidone Type B (~30 µm D50) manufactured in Pune, India. Its smaller particle size offers superior intragranular disintegration and is preferred in wet granulation processes where fine dispersion within the granule matrix is required. Ideal for direct compression formulations requiring uniform, fast disintegration. Meets USP/NF, EP, and IP specifications. Competitive pricing with full regulatory support for pharma manufacturers and exporters worldwide.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Crystalline Powder |
| Specific Optical Rotation | +54.4° To +55.9° |
| Loss On Drying | ≤ 0.5% |
| PH (10% W/v) | 4.0 – 6.5 |
| Residue On Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 5 Ppm |
| Clarity Of Solution | Clear, Colourless Solution |
| Microbial Limit | Complies USP <61> |
LACTISOL Lactose Monohydrate is a high-purity pharmaceutical excipient manufactured under WHO-GMP conditions in Pune, India. Available in multiple grades — crystalline (for wet granulation), spray-dried (for direct compression), and inhalation grade (DPI carrier) — meeting USP/NF, EP, and IP specifications. Its low hygroscopicity, chemical inertness, and pleasant mouthfeel make it the preferred diluent for DC tablets, dry powder inhalers (DPI), and capsule filling. A reliable, fully documented GMP-certified lactose monohydrate from India for pharmaceutical manufacturers.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Fine Powder |
| Degree Of Pregelatinization | ~20% (partially) |
| Loss On Drying | ≤ 14.0% |
| PH (10% Slurry) | 4.5 - 7.0 |
| Particle Size (D50) | 40 - 100 µm |
| Bulk Density | 0.45 - 0.65 G/mL |
| Compressibility Index | ≤ 20% |
| Heavy Metals | ≤ 10 Ppm |
MABITAB 1500 is a WHO-GMP and ISO 9001 certified partially pregelatinized starch (~20% pregelatinization) manufactured in Pune, India. It combines binder, disintegrant, and diluent functionality in a single excipient, directly compressible without requiring water — ideal for moisture-sensitive APIs. Meets USP/NF, EP, and IP specifications. Manufactured from maize starch with FSSAI, HALAL, and KOSHER certification. Competitive pricing with full regulatory documentation for pharma manufacturers in India and export markets.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Powder |
| Degree Of Pregelatinization | ≥ 80% (fully Pregelatinized) |
| Loss On Drying | ≤ 14.0% |
| PH (10% Slurry) | 4.5 – 7.0 |
| Particle Size (D50) | 50 – 150 µm |
| Cold Water Solubility | High |
| Bulk Density | 0.40 – 0.60 G/mL |
MABITAB 3000 is a WHO-GMP certified fully pregelatinized starch (≥80% pregelatinization) manufactured in Pune, India for pharmaceutical and food applications. Complete gelatinization delivers excellent cold-water solubility and dispersibility, superior DC binding, and disintegration performance. Suitable for direct compression tablets, reconstitutable dry powder suspensions, instant granules, sachets, and sustained-release matrices at higher concentrations. Meets USP/NF, EP, and IP specifications. ISO 22000, FSSAI, HALAL, KOSHER certified. Bulk supply from India with competitive pricing and full regulatory support.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Cream-coloured Hygroscopic Powder |
| K-value | 27.0 - 32.4 |
| Loss On Drying | ≤ 5.0% |
| PH (5% Solution) | 3.0 - 7.0 |
| Residue On Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 10 Ppm |
| Peroxide Value | ≤ 400 Ppm |
| Vinyl Pyrrolidone (monomer) | ≤ 10 Ppm |
POVIMINE K30 is a pharmaceutical-grade Polyvinylpyrrolidone (PVP K30 / Povidone K30) with a K-value of 27–32, manufactured under WHO-GMP and ISO 9001 conditions in Pune, India. It is the most widely used PVP grade for wet granulation binders, film coating, and solid dispersion formulations that enhance bioavailability of poorly soluble drugs (BCS Class II). POVIMINE K30 meets USP/NF, EP, and IP standards and is a WHO-GMP certified PVP K30 from India for regulated market filing. Supplied with full DMF support.
| Business Type | Manufacturer, Supplier, Retailer |
| Solubility | Freely Soluble In Water |
| Appearance | White To Creamy-white Hygroscopic Powder |
| Dextrose Equivalent (DE) | 10 - 20 |
| PH (10% Solution) | 4.0 - 7.0 |
| Loss On Drying | ≤ 5.0% |
| Sulphated Ash | ≤ 0.5% |
| Heavy Metals | ≤ 10 Ppm |
| Viscosity | Low (water-like In Solution) |
MALTOSURE is a WHO-GMP and ISO 9001 certified pharmaceutical-grade Maltodextrin (DE 5–20, maize/corn-derived) manufactured in Pune, India by controlled enzymatic hydrolysis. Available in multiple DE grades meeting USP/NF, EP, and IP specifications. With low hygroscopicity, neutral taste, and excellent flowability, MALTOSURE serves as a diluent, spray-drying carrier, and binder in solid dosage forms, nutraceuticals, orally disintegrating tablets (ODTs), and dry powder inhalation (DPI) formulations. HALAL, KOSHER, and FSSAI certified for dual pharma and food use. Bulk export from India to 50+ countries.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Cream Hygroscopic Powder Or Granule |
| K-value | 81.0 - 96.4 |
| Loss On Drying | <= 5.0% |
| PH (5% Solution) | 3.0 - 7.0 |
| Residue On Ignition | <= 0.1% |
| Heavy Metals | <= 10 Ppm |
| Vinyl Pyrrolidone (monomer) | <= 10 Ppm |
| Molecular Weight (Mw) | ~1,000,000 Da |
POVIMINE K90 is a high molecular weight Povidone (PVP K90, K-value 81–96) manufactured under WHO-GMP conditions in Pune, India. It offers superior film-forming and sustained-release matrix properties compared to lower K-value PVP grades. Preferred in extended-release tablets, ophthalmic drops, and topical viscosity-enhancing applications. POVIMINE K90 meets USP/NF, EP, and IP standards and is a WHO-GMP certified high-molecular-weight PVP K90 from India for pharmaceutical manufacturers. Active US-DMF support available.
| Business Type | Manufacturer, Supplier, Retailer |
| Degree Of Esterification | Low (LM) And High (HM) Grades Available |
| Loss On Drying | ≤ 12.0% |
| PH (1% Solution) | 2.8 - 3.8 |
| Galacturonic Acid Content | ≥ 74% |
| Heavy Metals | ≤ 20 Ppm |
| SO₂ | ≤ 50 Mg/kg |
| Viscosity | Grade-dependent |
MAPECTIN Pharma Grade Pectin is a high-purity natural polysaccharide (galacturonic acid ≥74%) extracted from citrus peels under WHO-GMP and ISO 9001 certified conditions in India, meeting USP/NF and EP pharmacopoeial standards. Available in Low Methoxyl (LM) for colon-targeted drug delivery systems (pH-sensitive, enzyme-degradable coating) and High Methoxyl (HM) for hydrophilic sustained-release tablet matrices and medicated gels. A natural, GRAS-status alternative to synthetic polymers for oral drug delivery. HALAL, KOSHER, ISO 22000, and FSSAI certified. Suitable for pharmaceutical, nutraceutical, and clean-label dietary supplement formulations. Bulk export from India.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White Fine Powder |
| Melting Range | 147 - 160°C |
| Assay (as Ca) | 6.4 - 7.4% |
| Loss On Drying | ≤ 4.0% |
| Particle Size (D50) | 10 - 30 µm |
| Heavy Metals | ≤ 10 Ppm |
| Acid Value | 196 - 211 Mg KOH/g |
| Microbial Limit | Complies USP <61> |
STEAREX Calcium Stearate is a WHO-GMP certified pharmaceutical-grade lubricant manufactured in Pune, India — the preferred alternative to magnesium stearate when Mg ions are contraindicated. Particularly suitable for effervescent tablets, calcium-supplemented formulations, and calcium-sensitive drug products. Also functions as an anti-caking agent in powder blends and as a mould release agent / heat stabilizer in PVC, polyolefin, and rubber processing. Meets USP/NF and EP specifications; HALAL and KOSHER certified. Available in controlled particle size (D50: 10–30 µm). Competitive pricing for pharma-grade and industrial-grade calcium stearate from India.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White To Off-white Fibrous Powder |
| Loss On Drying | ≤ 5.0% |
| PH (1% Suspension) | 5.0 - 7.5 |
| Degree Of Substitution | 0.05 - 0.49 |
| Bulk Density | ~0.25 G/mL |
| Heavy Metals | ≤ 10 Ppm |
| Microbial Limit | Complies USP <61> |
MYLCEL is a WHO-GMP certified Low-Substituted Hydroxypropyl Cellulose / Low-Substituted CMC-Na (L-HPC) manufactured in Pune, India — a multifunctional binder-disintegrant for wet granulation and direct compression. Its unique dual binder-disintegrant functionality reduces the total excipient count in a formulation — a single excipient provides both granule cohesion and tablet disintegration. Particularly effective in wet granulation processes where it improves granule strength while ensuring rapid tablet disintegration on contact with water. Meets USP/NF, EP, and JP pharmacopoeial specifications. HALAL, KOSHER certified. Bulk supply from India at competitive pricing with full regulatory documentation.
| Business Type | Manufacturer, Supplier, Retailer |
| Appearance | White, Unctuous Powder With Faint Odour |
| Melting Range | 117 - 150°C |
| Assay (as Mg) | 4.0 - 5.0% |
| Loss On Drying | ≤ 6.0% |
| Particle Size (D90) | ≤ 90 µm |
| Specific Surface Area | 1.5 - 14 M²/g |
| Heavy Metals | ≤ 10 Ppm |
| Source | Vegetable Grade Available |
STEARION Magnesium Stearate is a WHO-GMP certified, industry-standard pharmaceutical tablet lubricant manufactured in Pune, India and exported to 50+ countries. Available in both vegetable-derived (non-animal) and conventional grades to meet Halal, Kosher, and vegan formulation requirements. It prevents adherence of tablet material to punches and dies during compression, reduces inter-particulate friction, and ensures smooth tablet ejection. STEARION meets USP/NF, EP, and IP specifications and is supplied in controlled particle size fractions for optimal lubrication at competitive pricing from India.