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

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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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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:

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

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

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

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Applications:

SuperTab® 11SD offers the best compactability of all grades of lactose, and it is well suited to direct compression applications. Due to the low moisture content, it is used in the formulations containing moisture sensitive drugs.

Ingredient(s): Anhydrous Lactose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Ph. Eur., Lactose monograph / USP-NF, JP Anhydrous lactose monograph

Technical Specifications: Density- Tapped density- 906 g/l, Bulk density- 722 g/l; Particle size- D10-15 ?m, D50- 170 ?m, D90- 340 ?m; Hausner ratio-1,25

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Applications:

Solubilizing agents and Stabilizers.

Ingredient(s): Beta-Cyclodextrin

Dosage Form: Tablet

Category: Solubilizers, Thickeners and Stabilizers

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

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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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:

Tablet Coating, Rheology Modifier

Ingredient(s): Carboxymethyl cellulose sodium

Dosage Form: Tablet

Category: Coating Systems & Additives, Rheology Modifiers

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:

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:

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:

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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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:

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:

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:

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:

It provides solubility and viscosity stability on medium viscosity.

Ingredient(s): Carboxymethyl cellulose sodium

Dosage Form: Tablet

Category: Solubilizers, Thickeners and Stabilizers

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

Technical Specifications: Medium Viscosity

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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:

It provides smooth solutions, based on uniform substitution with low viscosity.

Ingredient(s): Carboxymethyl cellulose sodium

Dosage Form: Tablet

Category: Solubilizers, Thickeners and Stabilizers

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

Technical Specifications: Low Viscosity

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Applications:

It provides solubility and viscosity stability on strong high viscosity.

Ingredient(s): Carboxymethyl cellulose sodium

Dosage Form: Tablet

Category: Solubilizers, Thickeners and Stabilizers

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

Technical Specifications: Strong High Viscosity

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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:

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:

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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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:

Direct Compression

Ingredient(s): Anhydrous Lactose, Glyceryl Monostearate

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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Applications:

Standard Direct Tabletting Or Roller Compaction

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

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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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:

Direct Compression

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression & Granulations

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression & Granulations

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Dry Powder Inhalation

Ingredient(s): Anhydrous Lactose

Dosage Form: Inhaler

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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SODIUM CHLORIDE USP

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Applications:

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

Ingredient(s): Sodium Chloride Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: Not Available

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Applications:

Act as a bulk sweetener and vehicle in liquid dosage forms and as a humectant in semi solids.

Ingredient(s): Sorbitol liquid crystallizing

Dosage Form: Capsule, Suspension, Syrup, Tablet

Category: Fillers, Diluents & Binders, Taste Masking

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

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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Applications:

Suitable for use in biopharmaceutical manufacturing and as an excipient for injectable dosage forms

Ingredient(s): Sorbitol, 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:

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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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:

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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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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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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GLYCEROL MULTI-COMPENDIAL

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Applications:

A & C's Glycerol multi-compendial is an excipient that meets USP-NF, EP and BP monographs.

Ingredient(s): Glycerol Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: Not Available

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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: NF/EP/JP

Technical Specifications: Not Available

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Applications:

Wet Granulation & Capsule Filling

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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GLYCEROL USP

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Applications:

A & C's Glycerol is an excipient which meets the USP monograph.

Ingredient(s): Glycerol Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: Not Available

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Applications:

Wet Granulation & Capsule Filling

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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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:

Wet Granulation & Capsule Filling

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Filler, Diluent, & Bulking Agent In A Wide Variety Of Pharmaceutical Tablets, Capsules, Powders, And Other Preparations

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Ready mix sugar coating system.

Ingredient(s): Hydroxypropyl Methyl Cellulose, Sucrose, Titanium Dioxide

Dosage Form: Capsule, Tablet

Category: Coating Systems & Additives, Taste Masking

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

Technical Specifications: Sprayable sugar coating system for solid oral dosage form

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Applications:

Filler, Diluent, & Bulking Agent In A Wide Variety Of Pharmaceutical Tablets, Capsules, Powders, And Other Preparations

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Filler, Diluent, & Bulking Agent In A Wide Variety Of Pharmaceutical Tablets, Capsules, Powders, And Other Preparations

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Foremost™ Lactose 315 is a pharmaceutical excipient used in direct compression.

Ingredient(s): Lactose Monohydrate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Foremost Fast Flo® 316 is a pharmaceutical excipient used in direct compression.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Gohsenol EG acts as a pharmaceutical binder, filler and film former in various dosage forms like opthalmic, microsphere, OD strip and gel patches.

Ingredient(s): Polyvinyl Alcohol

Dosage Form: Capsule, Gel, Injectable / Parenteral, Ophthalmic Solution, Orodispersible Tablet, Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Parenteral, Topical

Route of Administration (Grade): Oral, Ophthalmic, Microsphere Injectable,Topical
Pharmacopoeia Reference: JPE, USP, EP, ChP (China)

Technical Specifications: Highly purified PVA, Partially hydrolysis, having all viscocity grade from 3cps to 48 cps.

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Flexible water soluble instant release coating polymer, especially used for moisture protection

Ingredient(s): Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer, Polyvinyl Alcohol

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

Category: Coating Systems & Additives, Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Excipient based on Kollicoat® IR and monographed raw materials

Technical Specifications: Not Available

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A pyrogen-free sorbitol used as a carbohydrate source and osmotic diuretic agent in large volume parenteral injectables.

Ingredient(s): Sorbitol

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: Not Available

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