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Anhui Sunhere Pharmaceutical Excipients Co.,Ltd

BASF

Corel Pharma Chem

DFE Pharma

Gangwal Chemicals

Lubrizol Life Science Health

Microlex e.U

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SPI Pharma

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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: Granule / Pellet, Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Direct Compression, Dry granulation

Ingredient(s): Microcrystalline Cellulose, STARCH, CORN

Dosage Form: Capsule, Granule / Pellet

Category: Granulation

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

Technical Specifications: Maize starch and Microcrystalline Cellulose

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Applications: Blend homogeneity even for low dose and micronized API’s, No need of other auxillary excipients

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Capsule, Granule / Pellet

Category: Granulation

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

Technical Specifications: Microcrystalline Cellulose and Colloidal Silicon Dioxide

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

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule, Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Direct Compression, Dry Granulation

Ingredient(s): Lactose Monohydrate, Microcrystalline Cellulose

Dosage Form: Capsule, Granule / Pellet

Category: Granulation

Route of Administration (Grade): Solid Oral
Pharmacopoeia Reference: IP, BP, USP-NF

Technical Specifications: Not Available

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Applications: Direct Compression, Dry Granulation

Ingredient(s): Anhydrous Lactose, Starch

Dosage Form: Capsule, Granule / Pellet

Category: Granulation

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

Technical Specifications: Maize starch and Lactose anhydrous

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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: Capsule, Orodispersible Tablet, Tablet

Category: Granulation

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

Technical Specifications: Not Available

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Applications: Direct Compression, Dry Granulation

Ingredient(s): Dibasic Calcium Phosphate, Microcrystalline Cellulose, Silicon Dioxide, Starch

Dosage Form: Capsule, Tablet

Category: Granulation

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

Technical Specifications: For small dose API and large dose API with good compressibility.

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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: Granule / Pellet, Orodispersible Tablet, 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: For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

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

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: Tablets, Granules, Pills, Disintegrants and fillers.

Ingredient(s): Crospovidone

Dosage Form: Granule / Pellet

Category: Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP/BP/EP/CP

Technical Specifications: Not Available

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Applications: HiCellac 100 is used in direct compression, dry granulation & capsule filling, suitable for low dose formulations where API content uniformity is critical. It also provides excellent compaction properties & tablet hardness.

Ingredient(s): Lactose Monohydrate, Microcrystalline Cellulose

Dosage Form: Tablet

Category: Granulation

Route of Administration (Grade): Oral
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: HiCel acts as a strong & dry binder. It facilitates low tablet friability & promotes rapid tablet disintegration.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Granulation

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

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: Granulation

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

Technical Specifications: Not Available

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Applications: AceCel is suitable for majority of the directly compressible actives, combines good flow and high compressibility.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Granulation

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

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: Granule / Pellet, 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: 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: Capsule, 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: It is used in oral pharmaceutical formulations as a super disintegrant for Capsules, Tablets & Granules Formulations. In tablet formulations, it is used in both direct compression & wet granulation processes.

Ingredient(s): Croscarmellose Sodium

Dosage Form: Tablet

Category: Granulation

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

Technical Specifications: Not Available

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

Category: Granulation

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

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: 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: Granule / Pellet, 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: 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): Palmitic Acid, Stearic Acid

Dosage Form: Granule / Pellet, 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 ODT solution with superior mouthfeel.

Ingredient(s): Crospovidone, Mannitol, Polyvinyl Acetate

Dosage Form: Orodispersible Tablet

Category: Granulation

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: Granule / Pellet, Tablet

Category: Granulation

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

Technical Specifications: Not Available