Pharmaceutical Excipients

AMBICEL MCC 101 is a WHO-GMP and ISO 9001 certified Microcrystalline Cellulose (MCC) with nominal particle size ~50 µm, meeting the pharmacopoeial MCC PH-101 grade specification. Manufactured at our MIDC Bhosari, Pune facility with active US-DMF, it meets USP/NF, EP, IP, JP, and ChP specifications. AMBICEL MCC 101 offers exceptional compressibility, binding, and compatibility for direct compression tablets, wet granulation, capsule filling, and extrusion-spheronisation. Available in bulk from India at competitive pricing. CoA, TDS, MSDS provided with every shipment. Export to 50+ countries since 1982.

AMBICEL MCC 102 is a WHO-GMP certified Microcrystalline Cellulose with nominal particle size ~90 µm, meeting the pharmacopoeial MCC PH-102 grade specification. Higher bulk density and superior flowability compared to MCC 101 make it the preferred grade for high-speed rotary tablet presses (>100,000 tablets/hour), continuous manufacturing lines, and high API-load formulations (≥70% API). Meets USP/NF, EP, IP, JP. US-DMF active. Exported from Pune, India to 50+ countries. Competitive bulk pricing with full documentation package.

AMBICEL MCC 112 is a WHO-GMP certified Silicified Microcrystalline Cellulose (SMCC) with ~90 µm particle size and ~2% colloidal silicon dioxide, meeting the pharmacopoeial SMCC specification. The silicification process imparts dramatically improved powder flow, moisture resistance, and anti-sticking properties vs. standard MCC 102. Ideal for moisture-sensitive APIs, high-humidity manufacturing environments, and high-speed tableting. Meets USP/NF and EP. Exported from Pune, India. Competitive SMCC price with full documentation.

AMBICEL MCC 200 is a WHO-GMP certified Microcrystalline Cellulose with ~180 µm particle size and low bulk density (0.22–0.30 g/mL), meeting the pharmacopoeial MCC PH-200 grade specification for extrusion-spheronisation pelletisation. Its unique plasticity imparts ideal rheological properties to wet masses, producing smooth, uniform spherical pellets for modified-release multiparticulate dosage forms, enteric-coated pellet capsules, and mini-tablets. Meets USP/NF, EP, and IP. Manufactured in Pune, India with active US-DMF. Ideal for pharmaceutical manufacturers seeking MCC PH-200 grade from India at competitive pricing.

AMBICEL MCC 301 is a WHO-GMP certified Microcrystalline Cellulose (~50 µm D50) manufactured in Pune, India, meeting the pharmacopoeial MCC PH-101 grade specification for compressibility and flowability. Ideal for direct compression and granulation. Meets USP/NF, EP, IP, and JP specifications. Suitable for tablets, capsules, and pelletisation. Full regulatory documentation (CoA, TDS, MSDS) and pharmacopoeial compliance certificate provided. HALAL, KOSHER certified. Bulk MCC supply from India at competitive pricing to 50+ countries.

AMBICEL MCC 302 is a WHO-GMP certified Silicified Microcrystalline Cellulose (SMCC, ~90 µm, ~2% SiO₂) manufactured in Pune, India. Co-processing with colloidal silicon dioxide imparts dramatically improved powder flow (Carr index <16%), moisture resistance, and anti-sticking properties vs. standard MCC — critical for moisture-sensitive APIs such as aspirin and effervescent blends. The preferred excipient when conventional MCC shows flow or sticking problems in high-humidity manufacturing environments or high-speed tablet presses. Meets USP/NF and EP; WHO-GMP, HALAL, KOSHER certified. Bulk supply from India.

AMB-MYL MBC 581 is a WHO-GMP certified Microcrystalline Cellulose (~50 µm D50) manufactured in Pune, India, meeting the USP/NF MCC PH-101 pharmacopoeial grade specification for particle size and performance. The AMB-MYL MBC range offers a dedicated low-moisture production line providing consistent lot-to-lot performance for pharmaceutical tablet manufacturers. Superior compressibility and binding capacity make it the workhorse excipient in direct compression and wet granulation worldwide. Meets USP/NF, EP, IP, and JP specifications. Full CoA, TDS, and regulatory documentation available. Exported from India to 50+ countries at competitive bulk pricing.

AMB-MYL MBC 591 is a WHO-GMP certified Microcrystalline Cellulose (~90 µm D50) manufactured in Pune, India, meeting the USP/NF MCC PH-102 pharmacopoeial grade specification. Larger particle size and higher bulk density (0.30–0.38 g/mL) vs MBC 581 delivers improved powder flow for high-speed rotary tablet presses (>100,000 tablets/hour) and high API-load formulations (≥70%). Preferred MCC grade for continuous tablet manufacturing lines. Meets USP/NF, EP, IP, and JP. Exported from India at competitive pricing with full pharmacopoeial documentation.

AMB-MYL MBC 611 is a WHO-GMP certified high-density Microcrystalline Cellulose (~110 µm D50) manufactured in Pune, India, delivering tablets with hardness >15 kP at modest compression forces. Exceptional compressibility minimises capping/lamination — ideal for challenging formulations with low-compressibility APIs. Preferred in chewable tablets (pleasant mouthfeel) and high-speed rotary presses. Meets USP/NF, EP, IP, JP. Full documentation package available. Exported from India to 50+ countries.

AMB-MYL MBC 811 is the ultra-high-density grade in the WHO-GMP certified AMB-MYL MCC series (~180 µm D50, bulk density 0.45–0.60 g/mL) — manufactured in Pune, India. Its best-in-class flowability reduces tablet press bowl volume requirements and improves manufacturing efficiency in continuous manufacturing and large-diameter tablet production. A premium granular MCC grade for demanding formulation challenges at competitive Indian pricing. Meets USP/NF, EP, IP, JP. CoA, TDS, MSDS supplied with every shipment.

AMBI-CELACT is a WHO-GMP certified co-processed excipient combining Microcrystalline Cellulose and Lactose Monohydrate (75:25 ratio, other ratios on request) for direct compression. Co-processing delivers superior compressibility, flowability, and batch consistency vs. physical mixtures of individual excipients. Ideal for high-speed tablet manufacture (>100,000 tabs/hour), nutraceuticals, and chewable tablets. Meets USP/NF and EP. Manufactured in Pune, India. Full regulatory documentation package available. Competitive co-processed excipient pricing from India.

AMBI-GG is a WHO-GMP certified co-processed excipient combining Microcrystalline Cellulose and Guar Gum, engineered for hydrophilic matrix tablets requiring controlled sustained drug release over 8–24 hours. The co-processing synergy delivers improved tablet hardness, reduced friability, and predictable drug-release kinetics compared to physical mixtures of individual components. A cost-effective co-processed matrix former for extended-release formulations — an alternative to Xcelodose or individual MCC + HPMC combinations in SR tablets. Ideal for pharmaceutical manufacturers seeking single co-processed excipient to simplify SR formulation development. Manufactured in Pune, India; USP/NF, EP compliant; HALAL, KOSHER certified.

AMBI-TCP is a WHO-GMP certified co-processed excipient combining Microcrystalline Cellulose with Tricalcium Phosphate (TCP) for direct compression supplement tablets. Uniquely suited for calcium supplement, multivitamin, and mineral tablet formulations where it delivers both excipient functionality (binding, filling) and the calcium active ingredient in a single directly compressible material. Eliminates the need for separate lubricants in many formulations; reduces excipient count and manufacturing steps. Available in customizable MCC:TCP ratios on request. Meets USP/NF; WHO-GMP, HALAL, KOSHER certified. Manufactured in Pune, India.

AMBICELOX is a pharmaceutical-grade Oxidised (Oxy-) Cellulose (Carboxyl content 18–24%) produced by selective nitrogen dioxide oxidation of high-purity cellulose under WHO-GMP conditions in Pune, India. Used as a resorbable haemostatic agent in surgical bleeding control (fully absorbed by the body within 7–14 days), as an absorbable wound matrix, and as a speciality pH-sensitive excipient in controlled-release formulations. Its biocompatibility, full biodegradability, and bacteriostatic properties in acidic pH make it preferred in surgical sponge, gauze, and topical haemostat applications. A quality-controlled alternative to imported oxidised cellulose products. Meets USP/NF and EP specifications; WHO-GMP and ISO 9001 certified.

AMYLAIZE is a WHO-GMP and ISO 9001 certified pharmaceutical-grade Maize (Corn) Starch meeting USP/NF, EP, and IP specifications, manufactured in Pune, India. One of the most globally used tablet excipients, it functions as a disintegrant (2–10%), wet granulation binder (as 5–15% starch paste), anti-adhesive dusting agent on tablet punches, and capsule shell component. AMYLAIZE is a natural alternative to branded maize starch excipients and dual-certified for pharmaceutical and food use (ISO 22000, FSSAI). Pharmaceutical buyers seeking corn starch USP/NF from India with full WHO-GMP documentation and competitive bulk pricing. HALAL, KOSHER certified. Exported to 50+ countries.

AMYLATO Pharmaceutical Grade Potato Starch is a WHO-GMP and ISO 9001 certified natural excipient conforming to USP/NF, EP, and IP specifications, manufactured in Pune, India. Derived from premium potato sources, it delivers excellent disintegration, binding (as a 5–10% starch paste), and lubrication in tablet and capsule manufacturing. Its high swelling capacity and compatibility with a broad range of APIs make it a cost-effective, clean-label natural starch excipient for pharmaceutical formulators. HALAL, KOSHER, ISO 22000, and FSSAI certified. Exported to 50+ countries with full pharmacopoeial documentation.

CARBOGENIX is a high-purity Sodium Carboxymethylcellulose (Na-CMC / Sodium CMC) manufactured under WHO-GMP and ISO 9001 conditions in Pune, India. Available in multiple viscosity grades (low, medium, high — 5 to 2000 mPa·s), it is widely used as a pharmaceutical binder, disintegrant, and suspending agent in tablet formulations, oral suspensions, gels, and topical preparations. CARBOGENIX meets USP/NF, EP, and IP standards and is a cost-effective, fully documented pharma-grade sodium CMC for solid and liquid dosage form manufacture. Exported to 50+ countries.

CEL-CA-CAL is a WHO-GMP and ISO 9001 certified pharmaceutical-grade Calcium Carboxymethyl Cellulose (Ca-CMC) — the insoluble calcium salt of CMC, manufactured in Pune, India and meeting USP/NF, EP, and IP specifications. Unlike sodium CMC (CARBOGENIX), CEL-CA-CAL is practically insoluble in water, functioning as a pH-independent matrix-forming binder and controlled-release disintegrant — ideal for sustained-release tablets, enteric systems, and formulations requiring drug release independent of GI fluid sodium content. Particularly suited when Na+ content must be minimized (cardiac, hypertensive patients). Degree of Substitution: 0.60–0.95; Calcium Content: 6.0–9.5%. HALAL, KOSHER certified. Full pharmacopoeial documentation available.

CEL-CA-DISSOL is a WHO-GMP certified crosslinked sodium carboxymethylcellulose (Croscarmellose Sodium) manufactured in Pune, India. Upon contact with water, it rapidly swells to over ten times its original volume, producing immediate tablet disintegration. Effective at concentrations of 1–3% in direct compression and 1–5% in wet granulation. Meets USP/NF, EP, and IP specifications with degree of substitution 0.60–0.85. Manufactured from cotton linters/wood pulp; full CoA, TDS, and DMF documentation available. Exported to 50+ countries.

CELTAB Sodium Starch Glycolate (SSG) is a WHO-GMP certified crosslinked potato starch super-disintegrant manufactured in Pune, India. It swells rapidly upon water contact (≥10× volume) to produce fast tablet disintegration. Low electrolyte sensitivity makes it compatible with most APIs and excipients. Meets USP/NF, EP, and IP specifications at 2–8% concentration for immediate-release tablets (direct compression and wet granulation). Degree of Substitution: 0.3–0.5; Sodium Content: 2.8–4.2%. Full pharmacopoeial documentation and US-DMF support available. Competitive pricing from Indian manufacturer exporting to 50+ countries.

CELVIA Pharmaceutical Grade Powdered Cellulose is a WHO-GMP and ISO 9001 certified α-cellulose powder (≥97%) manufactured by controlled mechanical processing of plant fibres in Pune, India. It serves as an inert filler, flow-aid, and adsorbent in tablet and capsule formulations. Available in multiple particle size grades (20–200 µm D50) for different compaction and flow requirements. A pharmacopoeial-grade powdered cellulose from India meeting USP/NF, EP, and IP; HALAL, KOSHER certified. Exported to 50+ countries.

COSILIFLOXA is a WHO-GMP and ISO 9001 certified pharmaceutical-grade Colloidal Silicon Dioxide (fumed silica) manufactured to meet USP/NF, EP, and IP standards in Pune, India. Its ultra-fine primary particle size (5–40 nm) and exceptionally high BET surface area (160–250 m²/g) make it the industry-standard glidant at 0.1–0.5% for improving powder flow in high-speed tablet compression and capsule filling. Also used as adsorbent for liquid APIs, anti-caking agent in dry powder blends, and rheology modifier in semi-solid topicals. HALAL, KOSHER certified. Exported to 50+ countries with full documentation.