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Aeon Procare

Anhui Sunhere Pharmaceutical Excipients Co.,Ltd

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Corel Pharma Chem

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Huzhou Sunflower Pharmacetuical Co. Ltd

Ideal Cures Pvt Ltd

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Kima Chemical

Microlex e.U

Nanjing Bold Chemical

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Qianhao Chemical (Hebei) Co., Ltd

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Shanghai Hegeng Industrial Co. Ltd

Shanghai Shenmei Pharmaceutical Technology Co., Ltd

Shanghai Welltone Material Technology Co., Ltd

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Virtual BoothYour partner for smart CDMO of intermediates and APIs, catalogue of intermediates & generic APIs, drug delivery solution

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Applications: Vitamin E TPGS (Tocophersolan) is a multirole excipient for pharmaceutical drug delivery. It can be used as a solubilizer for poorly soluble drugs and as an emulsifying agent, plasticizer, stabilizer & vehicle for lipid based formulations.

Ingredient(s): Tocophersolan

Dosage Form: Tablet

Category: Solubilizers

Route of Administration (Grade): Oral, Parenteral, Nasal, Ophthalmic, Topical
Pharmacopoeia Reference: USP 40 – NF 35

Technical Specifications: Specific Gravity: 1.06 at 50°C to 1.03 at 90°C; Solubility In Water: -20% at 20°C; Viscosity: 390cP at 50°C

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Applications: Pharmacel® 101 is a strong binder for wet & dry granulation formulations as it ensures uniform granulation and drying processes. It also provides excellent compaction and disintegration properties.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP, IP

Technical Specifications: Density- Tapped density- 440 g/l, Bulk density- 280 g/l; Particle size- D10- 25 ?m, D50- 60 ?m, D90- 20 ?m; Hausner ratio-1,57

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Applications: Pharmacel® 102 has good flow properties enabling high speed direct compression tableting. It is a ideal choice for direct compression & dry granulation formulations and it also has some lubrication properties for smooth tableting experience.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP, IP

Technical Specifications: Density- Tapped density- 440 g/l, Bulk density- 310 g/l; Particle size- D10- 40 ?m, D50- 90 ?m, D90-180 ?m; Hausner ratio-1,42

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Applications: SuperTab® 11SD is a highly consistent, spray-dried lactose enabling efficient tableting by offering free flow properties. It also offers excellent compaction properties & content uniformity.

Ingredient(s): Lactose Monohydrate Spray Dried

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP lactose monohydrate monograph

Technical Specifications: Density- Tapped density- 716 g/l, Bulk density- 599 g/l; Particle size- D10-50 ?m, D50- 120 ?m, D90- 220 ?m; Hausner ratio-1,2

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Applications: Primellose® croscarmellose sodium is an effective super-disintegrant ,suitable for a variety of tablet and capsule formulations. It is effective when used intragranular and/or extragranular in granular formulations.

Ingredient(s): Croscarmellose Sodium

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP

Technical Specifications: Not Available

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Applications: Pharmasperse® 416 Polyol Drug Delivery system is specifically enginered for the ready manufactue of orally dispersible powder(ODP) formulations

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Lubripharm® Sodium Stearyl Fumarate (SSF) is a tablet lubricant for use in traditional and orally disintegrating tablets, effervescent formulas, or in formulas where the active is incompatible with magnesium stearate.

Ingredient(s): Sodium Stearyl Fumarate Excipient

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Lubricants & Glidants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Adsorbent, Flow Aid, Moisture Protection, Stabilization of API

Ingredient(s): Magnesium Aluminometasilicate Type IA

Dosage Form: Tablet

Category: API Stability Enhancers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF, JP, EP

Technical Specifications: Not Available

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Applications: Orally Disintegrating Tablets/Sachets, Dispersible Tablets, Sachets, Chewable Tablets, Sublingual Tablets

Ingredient(s): Crospovidone, Dibasic Calcium Phosphate, Mannitol, Microcrystalline Cellulose, Xylitol Excipient

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Japanese Pharmaceutical Excipients. All components meet USP-NF, JP, and EP. US DMF Type IV filed.

Technical Specifications: Not Available

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Applications: Primojel® is a superdisintegrant suitable for a variety of tablet & capsule formulations. In higher concentrations, It can act as a dissolution enhancing agent.

Ingredient(s): Sodium Starch Glycolate

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP

Technical Specifications: Not Available

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Applications: Pharmatose® 200M is a highly consistent monohydrate lactose which delivers good compaction properties.This lactose type is typically used in tablets, capsules and extrusion spheronisation.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Fillers, Diluents & Binders, Granulation

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP lactose monohydrate monograph

Technical Specifications: Density- Tapped density- 857 g/l, Bulk density- 589 g/l; Particle size- D10- 5 ?m, D50- 40 ?m, D90- 120 ?m; Hausner ratio- 1,46

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Applications: SuperTab® 11SD offers the best compactability of all grades of lactose, and it is well suited to direct compression applications. Due to the low moisture content, it is used in the formulations containing moisture sensitive drugs.

Ingredient(s): Anhydrous Lactose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Ph. Eur., Lactose monograph / USP-NF, JP Anhydrous lactose monograph

Technical Specifications: Density- Tapped density- 906 g/l, Bulk density- 722 g/l; Particle size- D10-15 ?m, D50- 170 ?m, D90- 340 ?m; Hausner ratio-1,25

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Applications: Advantol® 300 Polyol Drug Delivery system is a directly compressible paltform to create soft chew or soft melt oral dosage forms.It is a robust system that allows fast product development.

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Direct Compression, Fillers, Diluents & Binders, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Adsorbent, Moisture Protection, Stabilization of API

Ingredient(s): Silicon Dioxide

Dosage Form: Tablet

Category: API Stability Enhancers, Thickeners and Stabilizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF, JP, EP

Technical Specifications: Also Available as FUJISIL-F

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Applications: Controlled Release, Direct Compression,Wet Granulation,Tablet Coating, Liquid Solutions and Suspensions

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: API Stability Enhancers, Coating Systems & Additives, Controlled & Modified Release, Direct Compression, Granulation, Rheology Modifiers

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Film Forming Agent, Wet/Dry Granulation- Binder,Thickening & Suspension Agent, Non-Gelatin Capsule Manufacturing & Enteric Film Coating Systems

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP, EP, and JP

Technical Specifications: Not Available

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Applications: Advantose® 100 is a spray-dried maltose powder that provides excellent flow, solubility, & tableting properties for oral dosage formulations. Maltose is well known for its safety & mouthfeel qualities, especially in chewable tablets & lozenges.

Ingredient(s): Maltose Sugar

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Direct Compression, Solubilizers, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Advantose® FS95 spray-dried fructose is coprocessed with a small quantity of starch, which results in a highly compressible excipient for pharmaceutical, nutraceutical, and chewable vitamin applications.

Ingredient(s): Fructose, Starch

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Direct Compression, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP, EP, and JP

Technical Specifications: Not Available

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Applications: Ready mix sugar coating system.

Ingredient(s): Hydroxypropyl Methyl Cellulose, Sucrose, Titanium Dioxide

Dosage Form: Tablet

Category: Coating Systems & Additives, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP / EP / JP & having US DMF

Technical Specifications: Sprayable sugar coating system for solid oral dosage form

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Applications: Binder, Film Former, Opthalmic, Microsphere, OD strip, Gel patches.

Ingredient(s): Polyvinyl Alcohol

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Oral, Ophthalmic, Microsphere Injectable,Topical
Pharmacopoeia Reference: JPE, USP, EP, ChP (China)

Technical Specifications: Highly purified PVA, Partially hydrolysis, having all viscocity grade from 3cps to 48 cps.

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Applications: Orally Disintegrating Tablets/Sachets, Dispersible Tablets/ Sachets, Chewable Tablets, Sublingual Tablets

Ingredient(s): Crospovidone, MAGNESIUM ALUMINOMETASILICATE, Mannitol, Microcrystalline Cellulose, Xylitol Excipient

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Japanese Pharmaceutical Excipients. All components meet USP-NF, JP, and EP.

Technical Specifications: Not Available

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Applications: Effer-Soda is a highly stable, surface modified sodium bicarbonate powder which eliminates formulation instability and expensive packaging to eliminate premature effervescence

Ingredient(s): Sodium Bicarbonate Excipient

Dosage Form: Tablet

Category: API Stability Enhancers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Compressol® SM polyol drug delivery system is a directly compressible platform consisting of mannitol and sorbitol. It assists the formulator with high active-loading formulations and difficult-to-compress actives.

Ingredient(s): Mannitol, Sorbitol

Dosage Form: Tablet

Category: Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Fillers, Diluents & Binders, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Diluent, Cushioning Agent

Ingredient(s): Dibasic Calcium Phosphate

Dosage Form: Tablet

Category: Direct Compression, Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF/EP/ JPC, US DMF Type IV, Listed as GRAS

Technical Specifications: Not Available

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Applications: Ready mix Film coating system for moisture sensitive APIs

Ingredient(s): Hydroxypropyl Methyl Cellulose, Microcrystalline Cellulose, Stearic Acid

Dosage Form: Tablet

Category: Coating Systems & Additives, Film Formers & Plasticizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP / EP / JP; Having US-DMF

Technical Specifications: Moisture barrier film coating system

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Applications: Diluent, Osmotic Tablets, Sustain Release Agent

Ingredient(s): Polyethylene Oxide

Dosage Form: Tablet

Category: Controlled & Modified Release, Direct Compression, Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF

Technical Specifications: Not Available

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Applications: Chemical structure was rationally designed to maximize safety and optimize interaction to improve the solubility, stability, bio availability or lessen volatility, irritation, smell or taste.

Ingredient(s): Betadex Sulfobutyl Ether Sodium Excipient

Dosage Form: Tablet

Category: Emulsifying Agents, Taste Masking, Thickeners and Stabilizers

Route of Administration (Grade): Parenteral, Oral, Ophthalmic, Nasal, Topical, Oral and Inhalation.
Pharmacopoeia Reference: USP NF

Technical Specifications: Captisol® is a polyanionic beta-cyclodextrin derivative with a sodium sulfonate salt separated from the lipophilic cavity by a butyl ether spacer group, or sulfobutylether (SBE). Relative to beta-cyclodextrin, Captisol® provides higher interaction charact

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Applications: Standard Direct Tabletting

Ingredient(s): Glyceryl Monostearate, Mannitol

Dosage Form: Tablet

Category: Co-Processed Excipients

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP

Technical Specifications: Not Available

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Applications: Stabilization/Complexation/Taste masking/Encapsulation/Odour masking

Ingredient(s): Hydroxypropyl Betacyclodextrin

Dosage Form: Tablet

Category: Solubilizers, Taste Masking, Thickeners and Stabilizers

Route of Administration (Grade): Solid/Liquid Oral/Inj/Opthalmic
Pharmacopoeia Reference: USP-NF / Ph. Eur. / BP / IP

Technical Specifications: Not Available

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Applications: Diluent; It improves hardness & disintegration

Ingredient(s): Maltose Sugar

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders

Route of Administration (Grade): Solid Orals, Liquids, Injections
Pharmacopoeia Reference: USP-NF, JPE, Type IV DMF

Technical Specifications: Maltose is a reducing disaccharide consisting of two glucose molecules linked by an ?-1,4 bond.

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Applications: Mannogem Mannitol products dissolve rapidly and can increase the rate of tablet disintegration and drug release. They can help accelerate tablet disintegration and subsequent drug dissolution.

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: API Stability Enhancers, Chewable & Orodispersible Aids, Direct Compression, Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications: Ready mix Non-Functional film coating system.

Ingredient(s): Hydroxypropyl Methyl Cellulose, polyethylene glycol, Talc Excipient

Dosage Form: Tablet

Category: Coating Systems & Additives, Film Formers & Plasticizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP / EP / JP; Having US-DMF

Technical Specifications: Ready mix Non-Functional film coating system

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Applications: Binder, Film Coating, SR polymer, solubility enhancement, topical spreading agent

Ingredient(s): Hydroxypropyl Cellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Fillers, Diluents & Binders, Film Formers & Plasticizers, Solubilizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Ingredient(s): Sucralose Excipient

Dosage Form: Tablet

Category: Taste Masking

Route of Administration (Grade): Oral Solids, Liquid Dosage
Pharmacopoeia Reference: IP/BP/EP/USP

Technical Specifications: Tastes similar to sugars. Smaller amount needed for same level of sweetening of sugar.They enhance flavours.

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Applications: Mannogem Mannitol products dissolve rapidly and can increase the rate of tablet disintegration and drug release. They can help accelerate tablet disintegration and subsequent drug dissolution.

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: API Stability Enhancers, Direct Compression, Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available