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Virtual BoothGlobal leader in Excipient Solutions

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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: Direct Compression

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

Technical Specifications: Not Available

Virtual BoothGlobal leader in Excipient Solutions

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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: 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: Direct Compression

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

Technical Specifications: Not Available

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Applications: Dry binder & fast disintegrant, suitable for small tablets and ODTs, providing pleasant mouthfeel due to finer particles.

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Tablet, Granule / Pellet, Orodispersible Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: Crospovidone Type B

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: Direct Compression

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: Direct Compression

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

Technical Specifications: Not Available

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

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet, Capsule

Category: Direct Compression

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

Technical Specifications: Not Available

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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: Direct Compression

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

Technical Specifications: Not Available

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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: Direct Compression

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

Technical Specifications: Not Available

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Applications: Pharmaburst® 500 Polyol Drug Delivery system is a directly compressible platform to create ODTs quickly & easily. It speeds developemnt time by providing a platform that only requires API, flavor and color to finalize a directly compressible formulation.

Ingredient(s): Mannitol

Dosage Form: Orodispersible Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications: Wetting agent, reducing disintegration time, direct compression, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Sodium Lauryl Sulfate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Sodium Laurilsulfate; USP-NF, JP: Sodium Lauryl Sulfate

Technical Specifications: Not Available

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Applications: Lipophilic lubricant, for sensitive acidic APIs, sustained release melt coating. Used as consistency factor to enhance the viscosity of topical formulations.

Ingredient(s): Hydrogenated Castor Oil

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., Castor Oil, hydrogenated, USP-NF: Hydrogenated Castor Oil, JP: Hydrogenated Oil

Technical Specifications: Not Available

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Applications: Lipophilic lubricant, for sensitive acidic APIs, Structure-building consistency factor for semi-solids, Viscosity regulator.

Ingredient(s): Stearyl Alcohol

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF, JP: Stearyl Alcohol

Technical Specifications: Not Available

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Applications: Solubilizer

Ingredient(s): Polysorbate 80, Magnesium Aluminometasilicate

Dosage Form: Tablet, Capsule, Dry Syrup

Category: Direct Compression

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

Technical Specifications: Solubilizer in powder form; EXCiPACT

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Applications: Lipophilic lubricant, especially for sensitive acidic APIs. Matrix forming agent in sustained-release dosage forms, emulsifying and solubilizing agent in topical formulations and hardening agent in glycerin suppositories

Ingredient(s): Stearic Acid, Palmitic Acid

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications: Solubilizer

Ingredient(s): Polyoxyl 40 hydrogenated castor oil

Dosage Form: Tablet, Capsule, Dry Syrup

Category: Direct Compression

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

Technical Specifications: Solubilizer in powder form; EXCiPACT

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Applications: Ready-to-use ODT solution with superior mouthfeel.

Ingredient(s): Polyvinyl Acetate, Crospovidone, Mannitol

Dosage Form: Orodispersible Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: 90 % mannitol, 5 % crospovidone, 5 % polyvinyl acetate

Technical Specifications: Not Available

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Applications: Ready-to-use direct compression solution for tablets.

Ingredient(s): Crospovidone, Lactose, Povidone

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph.Eur., USP/NF and JP

Technical Specifications: Not Available

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Applications: Ready-to-use direct compression solution for lozenges, chewables and effervescent tablets.

Ingredient(s): Povidone, Lactose

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP/NF and J.P

Technical Specifications: Not Available

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Applications: Capsule Filling, Direct Compression, Binding, Disintegration

Ingredient(s): Native & Pregelatinized Corn Starch

Dosage Form: Tablet, Capsule, Granule / Pellet

Category: Direct Compression

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

Technical Specifications: EXCiPACT

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Applications: Maximum disintegration

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: Crospovidone Type A

Technical Specifications: Not Available

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Applications: Balance of strong disintegration and optimal surface homogeneity.

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Orodispersible Tablet, Granule / Pellet, Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: Crospovidone Type A

Technical Specifications: Not Available

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Applications: Roller compaction & direct compression including slight disintegration functionality, Reduces sedimentation in suspensions. Solubilizer in transdermal patches.

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: Crospovidone Type B

Technical Specifications: Not Available

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Applications: For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

Ingredient(s): Lauryl Sulfate, Povidone, Polyvinyl Acetate, Hydrated Silica

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF, JP-JPE: 80 % Polyvinyl acetate and 19 % povidone, 0.8 % lauryl sulfate & 0.2 % silica (4:1)

Technical Specifications: Not Available

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Applications: Binder with fine particle size for roller compaction & direct compression

Ingredient(s): Vinylpyrrolidone-Vinyl Acetate Copolymer

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP monograph "Copovidone" and the JPE monograph "Copolyvidone"

Technical Specifications: Not Available

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Applications: Dry binder in tablets, capsules and granules, as a film-forming agent in tablet coatings and subcoatings, and as a film-forming agent in topical sprays. Widely used in HME processes.

Ingredient(s): Vinylpyrrolidone-Vinyl Acetate

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP monograph "Copovidone" and the JPE monograph "Copolyvidone"

Technical Specifications: Not Available

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Applications: Dissolution enhancer, lubricant & wetting agent, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Microprilled Poloxamer

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF: Poloxamer 188; JPE: Polyoxyethylene (160) Polyoxypropylene (30) glycol

Technical Specifications: Not Available

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Applications: Dissolution enhancer, lubricant & wetting agent, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Microprilled Poloxamer

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF: Poloxamer 407; JPE: Polyoxyethylene (196) Polyoxypropylene (67) glyco

Technical Specifications: Not Available

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Applications: Tablets made from these granules are typically easily disintegrated using conventional super disintegrates even when hard tablets are compressed.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Not Available

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Applications: The plastic defamation characteristics of  MCC 102 type mean that very hard tablets can be produced at light compaction forces, extending tooling lifetime and solving problems with poorly compressible actives.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Not Available

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Applications: Use in a wide range of oral applications such as wet or dry granulation, excipient of choice for flash release forms.

Ingredient(s): Mannitol

Dosage Form: Tablet, Capsule

Category: Direct Compression

Route of Administration (Grade): Topical, Oral
Pharmacopoeia Reference: Monograph- Ph.Eur, USP/NF

Technical Specifications: Available in different particle size as 25.µ, 50.µ, 180.µ

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Applications: Lactose monohydrate is typically used for wet or dry granulation. During wet granulation, liquid binders or adhesives are added to the lactose and active mixture, usually by blending.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Milled; Also Available as Microlex® LCM 180.m, Microlex® LCM 200.m

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Applications: It is also suitable for both wet granulation and direct compression methods of tablet production. Microlex® crystalline grades are used in wet granulation and the spray dried forms are used in direct compression.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Sieved; Also Available as Microlex® LCM 180.s, Microlex® LCM 220.s

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Applications: It is also suitable for both wet granulation and direct compression methods of tablet production. Microlex® crystalline grades are used in wet granulation and the spray dried forms are used in direct compression.

Ingredient(s): Anhydrous Lactose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Milled; Also Available as Microlex® LCA 120.m, Microlex® LCA 200.m

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Applications: Carbopol® 71G NF polymer is widely used in oral solid dose applications.The unique feature of this polymer is its granular form due to which it is used in direct compression formulations. The residual solvent in Carbopol 71G NF is Ethyl acetate.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet, Granule / Pellet

Category: Direct Compression

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type A, European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) monographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5) - 4,000 - 11,000

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Applications: Wet Granulation and Direct Compression

Ingredient(s): Polacrilin Potassium

Dosage Form: Tablet, Orodispersible Tablet, Capsule, Granule / Pellet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications: Wet Granulation and Direct Compression

Ingredient(s): Polacrilin Potassium

Dosage Form: Tablet, Orodispersible Tablet, Capsule, Granule / Pellet

Category: Direct Compression

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

Technical Specifications: Not Available

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