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Looking for NCGC00024579-04? Find NCGC00024579-04 based excipient solutions to address drug delivery challenges on PharmaCompass.

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01 Capsule (57)

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Applications:

KoVidone® K25 is used as a low viscosity wet binder.

Ingredient(s): Polyvinylpyrrolidone

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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Applications:

KoVidone® K30 is used as a binder for tablets and capsules.

Ingredient(s): Polyvinylpyrrolidone K30

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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Applications:

PolyKoVidone XL is used as a superdisintegrant and solid dispersant aid.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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Applications:

PolyKoVidone XL-10 is used as a superdisintegrant and solid dispersant aid.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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Applications:

PolyKoVidone Ultra XL is used as a superdisintegrant and solid dispersant aid.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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Applications:

PolyKoVidone Ultra XL-10 is used as a superdisintegrant and solid dispersant aid.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, EP, JP, KP, IP, BP

Technical Specifications: NA

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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:

Most popular excipient for the production of tablets and capsules. Offering an efficient and low dosage in capsules.

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

Technical Specifications: Specific Surface Area-6-10 m2/g; Particle Size-7-11 µm

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Applications:

Crospovidone is used as a disintegrant in solid oral dosage forms such as tablets and capsules.

Ingredient(s): Crospovidone

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: EP

Technical Specifications: Density?1.144g/cm3

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ACECEL

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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: Direct Compression, Fillers, Diluents & Binders, 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): Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone

Dosage Form: Capsule, Tablet, Topical Film, Transdermal Patch

Category: Controlled & Modified Release, Direct Compression, 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:

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:

It is used as an adhesive agent.

Ingredient(s): Povidone 30

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Also Available as K17, K25, K90 and VA-64

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HICEL

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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: Direct Compression, Fillers, Diluents & Binders, Granulation

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

Technical Specifications: Not Available

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Applications:

It is used as Tablet disintegrants

Ingredient(s): Sodium Starch Glycolate

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: Not Available

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Applications:

It is used as a filler in formulation.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Also Available as Comprecel M102, M102CG, M103, M105, M124, M113, M200, M224, M301, M302

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Applications:

Higher specific surface area and a smaller median particle size. This product is preferred for more critical and very fine herbal formulations.

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

Technical Specifications: Specific Surface Area-8-12 m2/g; Particle Size-5-9 µm

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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:

Tablets, Granules, Pills, Disintegrants and fillers.

Ingredient(s): Crospovidone

Dosage Form: Granule / Pellet, Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Granulation

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

Technical Specifications: Not Available

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Applications:

Pharmacel® 101 is a pharmaceutical excipient that acts as a pharmaceutical binder & filler for wet and dry granulation as it ensures uniform granulation and drying processes. It also provides excellent compaction and disintegration.

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:

Suitable for combination with the favourable crystalline. Designed for special formulations, as low and stable viscosity is required for tablet coatings, Supports a lower dissolution profile

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

Technical Specifications: Specific Surface Area-6-8 m2/g; Particle Size-7-11 µm

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Applications:

PVP K-30 is a non-ionic polymer used as a binder in oral solid dosage forms such as tablets.

Ingredient(s): PVP K 30

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Starch

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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HICEL MCC SPHERES

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Applications:

HiCel MCC Spheres are extremely versatile which is used for controlled release or sustained release formulations.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Lubricants, Anti-adhesive, Glidant

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

It is used as a lubricant.

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

Glidant; Emulsion Stabilizer; Anti-caking Agent.

Ingredient(s): Silicon Dioxide

Dosage Form: Tablet

Category: Emulsifying Agents, Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

Meets Kosher and Halal preparations in Jewish and Arab cultures. Qualified in high specification standards requested by European formulators.

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

It is used as a filler in formulation.

Ingredient(s): Corn Starch

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Tablet and capsule diluent, Tablet disintegrant.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/BP/EP/CP

Technical Specifications: Not Available

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Applications:

Tablet and capsule diluent, tablet and capsule disintegrant and tablet binder.

Ingredient(s): Corn Starch

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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HICEL SMCC

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Applications:

HiCel SMCC has unique combination which result in optimum compaction & superior flow properties.

Ingredient(s): Microcrystalline Cellulose, Silicon Dioxide

Dosage Form: Tablet

Category: Direct Compression, Fillers, Diluents & Binders, Lubricants & Glidants

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: Direct Compression, Granulation

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

Technical Specifications: Not Available

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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, 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:

Direct Compression

Ingredient(s): Glyceryl Monostearate, Microcrystalline Cellulose

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:

Direct Compression

Ingredient(s): Anhydrous Lactose, Glyceryl Monostearate

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:

Standard Direct Tabletting Or Roller Compaction

Ingredient(s): Anhydrous Lactose, Glyceryl Monostearate, Microcrystalline Cellulose

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:

Direct Tabletting Operations Where Fast Disintegration Is Required

Ingredient(s): Lactose, Microcrystalline Cellulose

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:

It facilitates to facilitate the dissolution of poorly API due to porous surface morphology.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants, Solubilizers

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

Technical Specifications: Also Available as Microlex® Cr.PVD CL-25, Microlex® Cr.PVD UCL-25, Microlex® Cr.PVD UCL-110

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Applications:

Orally Disintegrating Tablets

Ingredient(s): Crospovidone, Dextrose, Lactose, Mannitol

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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Applications:

Direct Compression

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression & Granulations

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression & Granulations

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Dry Powder Inhalation

Ingredient(s): Anhydrous Lactose

Dosage Form: Inhaler

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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SODIUM CHLORIDE USP

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Applications:

A & C's Sodium Chloride is an excipient meeting the USP monograph.

Ingredient(s): Sodium Chloride Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: USP

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: Capsule, 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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NACL MULTI-COMPENDIAL LOW ENDOTOXIN

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Applications:

A & C's Sodium Chloride multi-compendial low endotoxin is an excipient meeting USP-NF, EP, BP and JP monographs.

Ingredient(s): Sodium Chloride Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: Multi-compendial

Technical Specifications: Low Endotoxin

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Applications:

Ready-to-use direct compression solution for tablets.

Ingredient(s): Crospovidone, Lactose, Povidone

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression, 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): Lactose, Povidone

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression, 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:

Capsule Filling, Direct Compression, Binding, Disintegration

Ingredient(s): Native & Pregelatinized Corn Starch

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression

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

Technical Specifications: EXCiPACT

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Applications:

Solubilization, dispersion, crystallization inhibition, instant release matrices & spray drying

Ingredient(s): Povidone

Dosage Form: Capsule, Tablet, Transdermal Patch

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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KOLLIDON 30 LP

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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: Capsule, Granule / Pellet, Tablet

Category: Fillers, Diluents & Binders, Granulation

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

Technical Specifications: Not Available

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Applications:

Maximum disintegration

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Capsule, Granule / Pellet, Tablet

Category: Direct Compression, Disintegrants & Superdisintegrants

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

Technical Specifications: Not Available

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Applications:

Ludiflash is a ready-to-use orally disintegrating tablet (ODT) solution with superior mouthfeel.

Ingredient(s): Crospovidone, Mannitol, Polyvinyl Acetate

Dosage Form: Orodispersible Tablet

Category: Chewable & Orodispersible Aids, Direct Compression, 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:

It is a Co-Processed Lactose starch for filler/binder having strong disintegrant properties.

Ingredient(s): Corn Starch, Lactose

Dosage Form: Capsule, Tablet

Category: Co-Processed Excipients, Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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