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Looking for Timolol Maleate? Find Timolol Maleate based excipient solutions to address drug delivery challenges on PharmaCompass.

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Applications:

It stabilizes the pH of solutions. It is also an enzyme inhibitor used in the biopharmaceutical industry.

Ingredient(s): Tromethamine

Dosage Form: Cream / Lotion / Ointment, Injectable / Parenteral

Category: Parenteral, Topical

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

Technical Specifications: Bio Excipient Grade

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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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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:

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:

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 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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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:

Polysorbate 80 acts as solubilizer, emulsifier and wetting agent.

Ingredient(s): Polysorbate 80

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

Category: Solubilizers, Surfactant & Foaming Agents

Route of Administration (Grade): Oral, Topical & Parenteral
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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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:

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:

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:

Nonionic solubilizer, emulsifier and co-emulsifier

Ingredient(s): Polysorbate 80

Dosage Form: Gel, Softgel Capsule, Solution, Suppository

Category: Solubilizers

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

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:

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:

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:

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 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:

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:

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:

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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HYDROCHLORIC ACID NF

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Applications:

A&C's Hydrochloric Acid NF is used as a low pH neutralizing agent for pharmaceutical applications.

Ingredient(s): Hydrochloric Acid Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: 10% W/V

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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:

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:

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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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:

A & C's Polysorbate 80 multi-compendial is an excipient which meets USP-NF, EP, BP and JP monographs.

Ingredient(s): Polysorbate 80

Dosage Form: Capsule, Suspension, Tablet

Category: Solubilizers

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

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:

A & C's Polysorbate 80 is an excipient which meets the NF monograph.

Ingredient(s): Polysorbate 80

Dosage Form: Capsule, Suspension, Tablet

Category: Solubilizers

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

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:

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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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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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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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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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:

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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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:

Thickener, Emulsifier, Stabilizer, Texturizing agent, pH Independent & Non Thixotropic polymer for Topical Range (Skin,Vaginal & Anal mucosa)

Ingredient(s): Hydroxyethyl Acrylate, Polysorbate 80

Dosage Form: Cream / Lotion / Ointment, Emulsion

Category: Emulsifying Agents, Rheology Modifiers, Thickeners and Stabilizers, Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: In house having US DMF Type IV, IIG listed

Technical Specifications: Ready to use liquid polymer for topical applications (Gel / Cream / Lotion/ Foam based formulation, etc); It thickens over a wide range of pH 3-12; No HLB Calculation; No Neutralization

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Applications:

pH-independent sustained release coating for small particles, pellets, granules and tablets. Sprayable polymeric film former. Flexible. Wash resistant.

Ingredient(s): Polyvinyl Acetate, Sodium Lauryl Sulfate

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

Category: Coating Systems & Additives, Controlled & Modified Release, Taste Masking

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Poly(vinyl acetate) dispersion 30 per cent; USP: Polyvinyl Acetate Dispersion

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:

Solubilizer

Ingredient(s): Polysorbate 80, Polysorbate 80

Dosage Form: Capsule, Tablet, Dry Syrup

Category: Co-Processed Excipients, Direct Compression, Solubilizers

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

Technical Specifications: Solubilizer in powder form; EXCiPACT

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Applications:

Polysorbate 80 in dry powder form, a solubilizing agent acts as a surfactant and increases the solubility of various oral dosage forms.

Ingredient(s): Magnesium aluminium silicate Excipient, Polysorbate 80

Dosage Form: Tablet, Capsule

Category: API Stability Enhancers, Direct Compression, Solubilizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF, EP, JP & having US DMF

Technical Specifications: Solubilizer in powder form, used in directly compressible dosage forms, Wet granulation, added during lubrication stage

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Applications:

Self-emulsifying and consistency building, easy-to-use base for dermatological creams

Ingredient(s): Cetostearyl Alcohol, Sodium Cetostearyl Sulfate, Sodium Lauryl Sulfate

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

Category: Topical

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

Technical Specifications: Not Available

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

Ingredient(s): Mannitol

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

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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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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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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