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Anhydrous Lactose

Carbomer Homopolymer Type A

Crospovidone

Dried Corn Glucose Syrup

Ethyl Cellulose

EthylCellulose

Glucono delta lactone

Hydrogenated Castor Oil

Hydroxypropyl Methylcellulose

Lactose Monohydrate

Mannitol

Microcrystalline Cellulose

Microprilled Poloxamer

Pea Protein

Polacrilin Potassium

Poloxamer 188

Polyoxyl Hydogenated Castor Oil

Polyvinyl Acetate

Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer

Polyvinylpyrrolidone Crosslinked

Povidone

Sodium Lauryl Sulfate

Stearic Acid

Stearyl Alcohol

Vinylpyrrolidone-Vinyl Acetate

Vinylpyrrolidone-Vinyl Acetate Copolymer

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BASF

Corel Pharma Chem

DFE Pharma

Lubrizol Corporation

Microlex e.U

Roquette

SPI Pharma, Inc

The Dow Chemical Company

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AUSTRIA

FRANCE

GERMANY

INDIA

UNITED STATES

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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: 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: 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: Granulation

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

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): Povidone, Lauryl Sulfate, Polyvinyl Acetate, Hydrated Silica

Dosage Form: Tablet

Category: Granulation

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

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Moisture barrier, Multi particulates, Dry powder layering, Granulation, Hot melt extrusion, Taste Masking, Controlled / Modified Release

Ingredient(s): EthylCellulose

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Solubiliser, Plasticizer for coating & polymeric matrices, Nonionic emulsifier for O-W emulsions.

Ingredient(s): Polyoxyl Hydogenated Castor Oil

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur: Macrogolglycerol Hydroxystearate, USP-NF: Polyoxyl 40 hydrogenated castor oil

Technical Specifications: Not Available

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Applications: Wetting agent, reduces disintegration time, Ionic solubilizer, high HLB anionic emulsifier for semi-solids and foams.

Ingredient(s): Sodium Lauryl Sulfate

Dosage Form: Tablet

Category: Granulation

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

Ingredient(s): Sodium Lauryl Sulfate

Dosage Form: Tablet

Category: Granulation

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: Granulation

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: Granulation

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

Technical Specifications: Not Available

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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

Category: Granulation

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

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

Category: Granulation

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

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Increase solubility and bioavailability, Ideal for hot melt extrusion (HME)

Ingredient(s): Polyvinyl Acetate, polyethylene glycol

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Polyvinyl caprolactam – polyvinyl acetate – polyethylene glycol graft copolymer

Technical Specifications: Not Available

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Applications: Binder for peroxide sensitive drugs in solid oral dosage forms. Drug solubilizer with low peroxide in transdermal patches.

Ingredient(s): Povidone

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Tablet binding, Thickener, Stabilizers of suspensions, Reduces sedimentation, crystallization inhibition.

Ingredient(s): Povidone

Dosage Form: Tablet

Category: Granulation

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

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: Tablet

Category: Granulation

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

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

Category: Granulation

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

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

Category: Granulation

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

Ingredient(s): Vinylpyrrolidone-Vinyl Acetate Copolymer

Dosage Form: Tablet

Category: Granulation

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, drug solubilizer, plasticizer, thermoreversible gelling effect.

Ingredient(s): Poloxamer 188

Dosage Form: Tablet

Category: Granulation

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: For Instant Release Coating, Powerful and peroxide free wet binder for oxidation-sensitive drugs. Flexible and wash resistant film former in topical films.

Ingredient(s): Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Macrogol Poly(vinyl alcohol) Grafted Copolymer; USP-NF: Ethylene Glycol and Vinyl Alcohol Graft Copolymer; JPE: Methacrylic Acid Copolymer LD

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: Granulation

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: Granulation

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: Carbopol® 971P NF polymer is used in oral & mucosal contact applications such as extended/controlled release tablets, oral liquids, suspension & bioadhesive formulations. The residual solvent of Carbopol 971P NF is Ethyl acetate.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Granulation

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: 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: Granulation

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

Category: Granulation

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: Granulation

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: Granulation

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: Granulation

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: Wet Granulation and Direct Compression

Ingredient(s): Polacrilin Potassium

Dosage Form: Tablet

Category: Granulation

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

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It is widely used in oral solid, liquid dosage forms & topical formulations. It acts as excellent gel matrix former for controlling drug release in solid dosage forms.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF: Carbomer Homopolymer Type A, EP : Carbomers

Technical Specifications: Not Available

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Applications: Sustained Release, Taste Masking, Moisture Barrier, Binder in Wet Granulation

Ingredient(s): Ethyl Cellulose

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF: Ethyl cellulose dispersion Type B

Technical Specifications: Not Available

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Applications: It provides excipient benefits as a filler/binder while also providing nutrient benefits as a carbohydrate source.

Ingredient(s): Dried Corn Glucose Syrup

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It provides gentle acidification in cheese, minced meats, salad dressings and bakery products. After solubilization, GDL hydrolyzes slowly into gluconic acid.

Ingredient(s): Glucono delta lactone

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It provides gentle acidification in cheese, minced meats, salad dressings and bakery products. After solubilization, GDL hydrolyzes slowly into gluconic acid.

Ingredient(s): Glucono delta lactone

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It provides gentle acidification in cheese, minced meats, salad dressings and bakery products. After solubilization, GDL hydrolyzes slowly into gluconic acid.

Ingredient(s): Glucono delta lactone

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It provides nutrient benefits as a protein source for your nutraceutical product powder forms

Ingredient(s): Pea Protein

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It provides nutrient benefits as a protein source for your nutraceutical product powder forms

Ingredient(s): Pea Protein

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: It combines nutritional and technological advantages. It forms stable emulsions.

Ingredient(s): Pea Protein

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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