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Find excipient solutions to address Azithromycin formulation challenges (e.g. drug delivery, bioavailability, taste masking, controlled release, solubility, stability etc).

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Applications:

Tablet film coating, binders , main material of plant capsules.

Ingredient(s): Hypromellose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Film Formers & Plasticizers

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

Technical Specifications: Not Available

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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:

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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Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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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:

PLLA-PEG used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

Ingredient(s): Poly L Lactide, Polyethylene Glycol Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades

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TALC

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Applications:

Talc is a widely used as a dissolution retardant in the development of controlled release products. Talc is also used as a lubricant in tablet formulations.

Ingredient(s): Talc Excipient

Dosage Form: Granule / Pellet, Tablet

Category: Controlled & Modified Release, Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

A&C’s Benzalkonium Chloride 17% is a preservative which meets the NF monograph.

Ingredient(s): Benzalkonium chloride excipient

Dosage Form: Injectable / Parenteral, Tablet

Category: Solubilizers

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

Technical Specifications: 17% USP NF

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Applications:

It is used in producing the injection solution, reducing the encephalic pressure, the intraocular pressure etc.

Ingredient(s): Mannitol

Dosage Form: Injectable / Parenteral, Tablet

Category: Fillers, Diluents & Binders, Parenteral

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

Technical Specifications: Pharma Grade/ Medicine Grade/Injectable Grade

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Applications:

PLGA-PEG is used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

Ingredient(s): Poly-DL-Lactic-co-Glycolic Acid, Polyethylene Glycol Excipients

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades.

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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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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:

Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule, 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:

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:

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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BENZALKONIUM CHLORIDE

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Ingredient(s): Benzalkonium chloride excipient

Dosage Form: Nasal Solution, Ophthalmic Solution

Category: Parenteral

Route of Administration (Grade): Ophthalmic and Nasal
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

It is used as a filler in formulation.

Ingredient(s): Mannitol

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:

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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POLYETHYLENE GLYCOL 400 NF

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Ingredient(s): polyethylene glycol

Dosage Form: Capsule, Cream / Lotion / Ointment, Gel, Tablet

Category: Controlled & Modified Release, Topical

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

Technical Specifications: Not Available

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PHARMATOSE 200M

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Applications:

Pharmatose® 200M is a pharmaceutical excipient that is a highly consistent monohydrate lactose which delivers good compaction properties. This lactose type is typically used in oral dosage forms like tablets and pharmaceutical capsules.

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, 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:

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:

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:

Instamodel Blend is used to provide Extended Release from the dosage form.

Ingredient(s): HPMC 2910

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:

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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COLORCOAT MB4S(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Lactose Monohydrate

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:

Polyglykol 4000 PF is a milled PEG excipient grade powder product with a fine particle size distribution which is used as binder in oral dosage forms.

Ingredient(s): Polyethylene Glycol 4000

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

Route of Administration (Grade): Topical
Pharmacopoeia Reference: USP-NF: Polyethylene glycol 4000, Ph. Eur.: Macrogol 4000

Technical Specifications: average molar mass 4000 g/mol

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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:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

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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COLORCOAT FC4S

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Applications:

Film Coating

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar, Polyvinyl Alcohol

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

Route of Administration (Grade): Not Available
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:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

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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Applications:

It is used as a disintegrating agent.

Ingredient(s): Croscarmellose Sodium

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: Also Available as Disolcel® GF

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Lactose

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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Applications:

Tablet and capsule disintegrant.

Ingredient(s): Croscarmellose Sodium

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants

Route of Administration (Grade): Oral
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): 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:

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:

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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COLORCOAT FC4W

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Applications:

Film Coating

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar, Polyvinyl Alcohol

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

Route of Administration (Grade): Not Available
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: Capsule, Tablet

Category: Direct Compression, Granulation, Lubricants & Glidants

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:

Immediate Release

Ingredient(s): Polyvinyl Alcohol

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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Applications:

It is used as an adhesive agent.

Ingredient(s): Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Also Available as AnyCoat®-C AN3, AN4, AN5, AN6, AN15, AN50, BN4

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Applications:

An immediate-release HPMC capsule without gelling agents. Vcaps® Plus offer excellent dissolution profile with pH-independent performance, standard or low-moisture content, great machinability and visual quality.

Ingredient(s): Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: API Stability Enhancers, Vegetarian Capsules

Route of Administration (Grade): Oral and Inhalation
Pharmacopoeia Reference: Certified Vegan, Non-GMO, Vegetarian Society, Halal and Kosher certifications

Technical Specifications: "Water content – less than 9%, can be customized; Size # 00el - 4

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Applications:

Tablet binders and disintegrants

Ingredient(s): Croscarmellose Sodium

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

A & C's Maltodextrin is an excipient which meets the NF monograph.

Ingredient(s): Maltodextrin Excipient

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

Category: Solubilizers

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

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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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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Applications:

It offers an enteric-release profile to the upper gastro-intestinal tract that meets the disintegration requirements for delayed-release capsules for the European, US and Japanese Phamacopoeia.

Ingredient(s): HPMC AS, Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: Controlled & Modified Release, Vegetarian Capsules

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Complies with relevant European, Japanese and US Pharmacopeia monographs

Technical Specifications: Water content – less than 6%; Size #0

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Applications:

Direct Compression

Ingredient(s): Glyceryl Monostearate, Spray Dried Monohydrate Lactose

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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COLORCOAT FC4WS

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Applications:

Film Coating

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar, Polyvinyl Alcohol

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Glycerol, Unmodified, Hydroxypropyl Methylcellulose

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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Applications:

Plasticizer particularly suitable for tablet coatings. Versatile water or oil miscible solvent in topical formulations.

Ingredient(s): Triacetin

Dosage Form: Capsule, Tablet

Category: Film Formers & Plasticizers

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

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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POLYETHYLENE GLYCOL 200 NF

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Applications:

A & C's Polyethylene Glycol 200 is an excipient which meets the NF monograph.

Ingredient(s): polyethylene glycol

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

Route of Administration (Grade): Parenteral, Topical
Pharmacopoeia Reference: NF

Technical Specifications: Polyethylene Glycol 200; Polyethylene Glycol 300; Polyethylene Glycol 400; Low Endotoxin

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar

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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COLORCOAT FC4W(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

Forms anhydrous, hydrophilic ointments in combination with low mol. weight PEG

Ingredient(s): Polyethylene Glycol 8000

Dosage Form: Cream / Lotion / Ointment, Emulsion, Gel, Suppository

Category: Thickeners and Stabilizers, Topical

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

Technical Specifications: Not Available

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POLYETHYLENE GLYCOL 300 NF

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Applications:

A & C's Polyethylene Glycol 300 is an excipient which meets the NF monograph.

Ingredient(s): polyethylene glycol

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

Route of Administration (Grade): Topical, Parenteral
Pharmacopoeia Reference: NF

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: Direct Compression, 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:

Protein Stabilization, Lyo & Cryo, stabilization, Vaccine Stabilization, Bulking Agent

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: Fillers, Diluents & Binders, Thickeners and Stabilizers

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

Technical Specifications: Not Available

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POLYETHYLENE GLYCOL 400 NF

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Applications:

A&C's Polyethylene Glycol 400 USP-NF is a short chain non-ionic surfactant.

Ingredient(s): polyethylene glycol

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

Route of Administration (Grade): Topical, Parenteral
Pharmacopoeia Reference: Not Available

Technical Specifications: Low Endotoxin

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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, 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:

Cell Culture & Bioprocessing, Bulking Agent, Protein Stabilization, Lyo & Cryo stabilization, Vaccine Stabilization

Ingredient(s): Sucrose

Dosage Form: Emulsion, Solution, Suspension, Syrup, Tablet

Category: Thickeners and Stabilizers

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

Technical Specifications: Not Available

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COLORCOAT FC4S(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): Ethyl Cellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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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:

It is used in film coating of tablets due to its higher molecular weight and higher resistance to simulated gastric fluid, high degree of polymerisation.

Ingredient(s): Hypromellose

Dosage Form: Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Also Available as Microlex® HML C2906, Microlex® HML C2208.

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COLORCOAT MB4W

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Applications:

Moisture Barrier Coating

Ingredient(s): Ethyl Cellulose, Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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FILLERLAC

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Applications:

Lactose is widely used as a filler and diluent in tablets and capsules, and to a more limited extent in lyophilized products and infant formulas.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression, Fillers, Diluents & Binders

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

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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COLORCOAT MB4S

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Applications:

Moisture Barrier Coating

Ingredient(s): Ethyl Cellulose, Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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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:

Noveon® polycarbophil provides excellent bioadhesive properties & can be used for the formulation of buccal, nasal, ophthalmic, rectal bioadhesive products. lt can also be used as a controlled release polymer in oral solid dose applications.

Ingredient(s): Polycarbophil

Dosage Form: Solution, Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Topical, Oral, Nasal & Ophthalmics
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Polycarbophil.

Technical Specifications: Viscosity, cP (0.2 wt% at pH 7.5) - 2,000 - 12,000

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COLORCOAT SC4W

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Applications:

Seal Coating

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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COLORCOAT SC4S

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Applications:

Seal Coating

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

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:

Enteric Coatings

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

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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SODIUM CITRATE DIHYDRATE MULTI-COMPENDIAL

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Applications:

A & C's Sodium Citrate Dihydrate multi-compendial is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

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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SODIUM CITRATE DIHYDRATE USP-NF

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Applications:

A & C's Sodium Citrate Dihydrate USP-NF is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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ACRYCOAT E100

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Applications:

Moisture Barrier

Ingredient(s): Amino Methacrylate Copolymer

Dosage Form: Capsule, Tablet

Category: Film Formers & Plasticizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF: Amino Methacrylate Copolymer - NF

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Lecithin, Polyvinyl Alcohol

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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ACRYCOAT EPO

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Applications:

Taste Masking

Ingredient(s): Amino Methacrylate Copolymer

Dosage Form: Tablet

Category: Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF: Amino Methacrylate Copolymer - NF

Technical Specifications: Not Available

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MICROLEX® ML-INJ 500

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Applications:

It is used as Diurectic-osmotic for injectable solution, Dialysis solution, Injectible and Parenteral solution.

Ingredient(s): Mannitol

Dosage Form: Injectable / Parenteral, Solution

Category: Parenteral

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: Monograph- Ph.Eur, USP/NF, JP/JPE, FDA IIG

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose

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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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

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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PEARLITOL® BIOPHARMA

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Applications:

Its range offers a unique blend of exceptional physical and chemical stability and no hygroscopicity.

Ingredient(s): Mannitol, low endotoxin

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

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: Capsule, Tablet

Category: Coating Systems & Additives, Film Formers & Plasticizers

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

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: Capsule, Tablet

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

Dry Powder Inhalation

Ingredient(s): Lactose Monohydrate

Dosage Form: Inhaler

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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