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Looking for Prestwick3_000447? Find Prestwick3_000447 based excipient solutions to address drug delivery challenges on PharmaCompass.

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Applications:

Sorbiplast (Sorbitol) is used as a plasticizer that provides the required elasticity in soft-gelatin capsules.

Ingredient(s): Sorbitol

Dosage Form: Softgels

Category: Film Formers & Plasticizers

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

Technical Specifications: NA

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Applications:

Castor oil is used as an oily solvent in parenteral dosage forms.

Ingredient(s): Castor Oil Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: USP/EP/JP

Technical Specifications: NA

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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:

Calcium stearate is used as lubricants and glidants in the formulation of tablets and capsules.

Ingredient(s): Calcium Stearate

Dosage Form: Capsule, Tablet

Category: Lubricants & Glidants

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

Technical Specifications: NA

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L-(+)-LACTIC ACID

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Ingredient(s): L Lactic Acid

Dosage Form: Gel, Injectable / Parenteral

Category: Parenteral, Topical

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

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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BENZYL ALCOHOL MULTI-COMPENDIAL

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Applications:

A&C’s Benzyl Alcohol multi-compendial is a preservative which meets USP-NF, EP, BP and JP monographs.

Ingredient(s): Benzyl Alcohol Excipient

Dosage Form: Cream / Lotion / Ointment

Category: Topical

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

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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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:

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:

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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PROPYLENE GLYCOL

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Ingredient(s): Propylene Glycol

Dosage Form: Capsule, Cream / Lotion / Ointment

Category: Film Formers & Plasticizers, Topical

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

Technical Specifications: Not Available

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Applications:

Nonionic solubilizer, emulsifier and co-emulsifier

Ingredient(s): Polysorbate 20

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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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:

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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UREA

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Ingredient(s): Urea

Dosage Form: Cream / Lotion / Ointment

Category: Topical

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

Technical Specifications: Not Available

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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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2-PHENOXYETHANOL PHEUR

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Applications:

A & C's 2-Phenoxyethanol is used as an excipient and meets the EP monograph

Ingredient(s): 2-Phenoxyethanol Excipient

Dosage Form: Cream / Lotion / Ointment

Category: Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: PhEur

Technical Specifications: Not Available

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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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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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Applications:

Polyglykol 400 is a liquid PEG excipient grade product which is used as solvent, humectant, coating agent and viscosity enhancer.

Ingredient(s): Polyethylene Glycol 400

Dosage Form: Cream / Lotion / Ointment, Emulsion

Category: Coating Systems & Additives, Rheology Modifiers, Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: USP-NF: Polyethylene glycol 400, J.P.: Macrogol 400, Ph. Eur.: Macrogol 400

Technical Specifications: average molar mass 400 g/mol

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Applications:

Nonionic solubilizer, emulsifier and co-emulsifier

Ingredient(s): Polysorbate 60

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:

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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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:

A & C's Benzethonium Chloride USP is a hygroscopic excipient, which meets USP requirements.

Ingredient(s): Benzethonium Chloride Exc

Dosage Form: Injectable / Parenteral, Tablet

Category: Solubilizers

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

Technical Specifications: 17% USP NF; 50% NF; USP

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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:

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:

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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MAGNESIUM ALUMINIUM SILICATE

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Applications:

Magnesium aluminium silicate is used as opacifying agent, anticaking agent, viscosity agent, suspending agents.

Ingredient(s): Magnesium aluminium silicate Excipient

Dosage Form: Suspension, Tablet

Category: Lubricants & Glidants, Thickeners and Stabilizers

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

Technical Specifications: Not Available

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BENZYL ALCOHOL

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Ingredient(s): Benzyl Alcohol

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

Category: Parenteral, Topical

Route of Administration (Grade): Parenteral and Topical
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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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:

It is used as a lubricant.

Ingredient(s): Calcium 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:

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:

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

Ingredient(s): Polyoxyl Hydogenated Castor Oil

Dosage Form: Capsule, Emulsion, Softgel Capsule, Tablet

Category: Film Formers & Plasticizers, Granulation, Solubilizers

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:

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:

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:

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:

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:

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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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:

Non-Ionic Hydrophilic Surfactant, Emulsifier

Ingredient(s): Polysorbate 60

Dosage Form: Capsule, Cream / Lotion / Ointment, Gel, Shampoo, Solution, Syrup

Category: Emulsifying Agents, Topical

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

Technical Specifications: HLB: 15, EO: 20; EXCiPACT

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Stearic acid is a saturated, wax-like, fatty acid commonly used in the production of pharmaceutical tablets and capsules.

Ingredient(s): Stearic Acid

Dosage Form: Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

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:

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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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:

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 water repellent agent in the production of effervescent tablets to to prevent unwanted absorption of moisture.

Ingredient(s): Calcium Stearate

Dosage Form: Tablet

Category: Lubricants & Glidants

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

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

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Applications:

Solvent for lipophilic drugs

Ingredient(s): Cetearyl Ethylhexanoate, Isopropyl Myristate

Dosage Form: Emulsion, Solution

Category: Topical

Route of Administration (Grade): Not Available
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): Calcium Stearate

Dosage Form: Tablet

Category: Lubricants & Glidants

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

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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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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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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PHENYL ETHYL ALCOHOL MULTI-COMPENDIAL

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A & C's Phenyl Ethyl alcohol is a preservative that meets USP-NF and JP monographs.

Ingredient(s): Phenylethyl Alcohol 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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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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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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PHENYL ETHYL ALCOHOL USP

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A & C's Phenyl Ethyl alcohol is an excipient which meets the USP monograph.

Ingredient(s): Phenylethyl Alcohol Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

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:

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: Cream / Lotion / Ointment, Granule / Pellet, Suspension, Tablet

Category: Controlled & Modified Release, Granulation, Thickeners and Stabilizers, Topical

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:

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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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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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:

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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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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A & C's Polysorbate 20 is an excipient which meets the NF monograph.

Ingredient(s): Polysorbate 20

Dosage Form: Capsule, Cream / Lotion / Ointment, Tablet, Topical Film

Category: Solubilizers

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

Technical Specifications: Not Available

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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:

Carbopol® 974P NF polymer is used in oral and mucosal contact applications such as oral liquids, bioadhesive formulations, & extended release tablets. Additionally, it can be used to formulate viscous gels, emulsions & suspensions.

Ingredient(s): Carbomer Homopolymer Type B

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

Category: Controlled & Modified Release, Topical

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type B, European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) mongographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 29,400 - 39,400

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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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COLORCOAT MB4W

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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:

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:

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:

Carbopol® 940 NF polymer is a highly efficient thickener used for formulating clear aqueous and hydroalcoholic gels. The polymer has short flow rheology similar to mayonnaise.

Ingredient(s): Carbomer 940 Excipient

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer 940

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 40,000 - 60,000

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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:

Pemulen™ TR-2 NF polymer is a primary oil-in-water emulsifier which can emulsify up to 50% oil by weight. It delivers the topical medication in the form of low-irritancy lotions, creams & for high-clarity topical gels.

Ingredient(s): Carbomer Copolymer Type A

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

Category: Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Copolymer Type A

Technical Specifications: Viscosity, cP (1.0 wt% at pH 7.5) - 4,500 - 13,500

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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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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:

Carbopol® 980 NF is highly efficient thickener and ideal excipient for formulating clear aqueous and hydroalcoholic gels. The residual solvent for Carbopol 980 NF is cosolvent mixture of ethyl acetate and cyclohexane.

Ingredient(s): Carbomer Homopolymer Type C

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Thickeners and Stabilizers, Topical

Route of Administration (Grade): Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type C. European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) monographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 40,000 - 60,000

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Applications:

Large Volume Parenterals

Ingredient(s): Sodium S Lactate

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

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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