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Looking for NCGC00024409-09? Find NCGC00024409-09 based excipient solutions to address drug delivery challenges on PharmaCompass.

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01 Nanjing Well Pharmaceutical (5)

02 Rochem International Inc (5)

03 SPI Pharma (6)

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31 Shanghai Shenmei Pharmaceutical Technology Co., Ltd (6)

32 Sigachi Industries (2)

33 The Dow Chemical Company (3)

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35 Vasa Pharmachem (1)

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01 Capsule (68)

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Applications:

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

Ingredient(s): Polyvinylpyrrolidone

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: NA

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Applications:

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

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: NA

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Applications:

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

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: NA

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Applications:

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

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: NA

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Applications:

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

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: NA

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Applications:

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:

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:

For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

Ingredient(s): Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone

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

Category: Controlled & Modified Release, Direct Compression, Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF, JP-JPE: 80 % Polyvinyl acetate and 19 % povidone, 0.8 % lauryl sulfate & 0.2 % silica (4:1)

Technical Specifications: Not Available

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Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Crospovidone

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: Density?1.144g/cm3

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Applications:

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

Ingredient(s): Hypromellose

Dosage Form: Capsule, Tablet

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

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

Technical Specifications: Not Available

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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:

Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule, Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

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

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Applications:

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:

Tablets, Granules, Pills, Disintegrants and fillers.

Ingredient(s): Crospovidone

Dosage Form: Granule / Pellet, Tablet

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

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

Technical Specifications: Not Available

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Applications:

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:

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

Ingredient(s): HPMC 2910

Dosage Form: Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Starch

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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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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COLORCOAT MB4S(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

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:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

It is used as a 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:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Magnesium Stearate

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders, Lubricants & Glidants

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, 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:

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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COLORCOAT FC4W

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Applications:

Film Coating

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

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

Wetting agent, reducing disintegration time, direct compression, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Sodium Lauryl Sulfate

Dosage Form: Capsule, Tablet

Category: Direct Compression, Granulation, Lubricants & Glidants

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Sodium Laurilsulfate; USP-NF, JP: Sodium Lauryl Sulfate

Technical Specifications: Not Available

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Applications:

It is used as an adhesive agent.

Ingredient(s): Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

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

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Applications:

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

Ingredient(s): Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: API Stability Enhancers, Vegetarian Capsules

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

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

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): HPMC AS, Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: Controlled & Modified Release, Vegetarian Capsules

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

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

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Applications:

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

Ingredient(s): Corn Starch

Dosage Form: Capsule, Tablet

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Direct Compression

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

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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COLORCOAT FC4WS

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Applications:

Film Coating

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

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Glycerol, Unmodified, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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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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COLORCOAT FC4W(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Polyethylene Glycol 8000

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

Category: Thickeners and Stabilizers, Topical

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

Technical Specifications: Not Available

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POLYETHYLENE GLYCOL 300 NF

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Applications:

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

Ingredient(s): polyethylene glycol

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

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

Technical Specifications: Not Available

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Applications:

Lactose monohydrate is typically used for wet or dry granulation. During wet granulation, liquid binders or adhesives are added to the lactose and active mixture, usually by blending.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression, Granulation

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

Technical Specifications: Milled; Also Available as Microlex® LCM 180.m, Microlex® LCM 200.m

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POLYETHYLENE GLYCOL 400 NF

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Applications:

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

Ingredient(s): polyethylene glycol

Dosage Form: Cream / Lotion / Ointment, Gel

Category: Topical

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

Technical Specifications: Low Endotoxin

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Applications:

It is also suitable for both wet granulation and direct compression methods of tablet production. Microlex® crystalline grades are used in wet granulation and the spray dried forms are used in direct compression.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression, Granulation

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

Technical Specifications: Sieved; Also Available as Microlex® LCM 180.s, Microlex® LCM 220.s

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COLORCOAT FC4S(CLEAR)

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Applications:

Transparent Coating

Ingredient(s): Ethyl Cellulose, Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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Applications:

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): 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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Applications:

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

Ingredient(s): Hypromellose

Dosage Form: Tablet

Category: Coating Systems & Additives

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

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

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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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FILLERLAC

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LM Application #LearnMore

Applications:

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

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression, Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications:

Standard Direct Tabletting Or Roller Compaction

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

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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COLORCOAT MB4S

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LM Application #LearnMore

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:

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

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Disintegrants & Superdisintegrants, Solubilizers

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

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

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Applications:

Orally Disintegrating Tablets

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

Dosage Form: Tablet

Category: Co-Processed Excipients

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

Technical Specifications: Not Available

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Applications:

Direct Compression

Ingredient(s): Anhydrous Lactose

Dosage Form: Capsule, Tablet

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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COLORCOAT SC4W

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LM Application #LearnMore

Applications:

Seal Coating

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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COLORCOAT SC4S

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LM Application #LearnMore

Applications:

Seal Coating

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: Not Available

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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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LM Application #LearnMore

Applications:

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

Ingredient(s): Sodium Chloride Excipient

Dosage Form: Injectable / Parenteral

Category: Parenteral

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

Technical Specifications: Not Available

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Applications:

Enteric Coatings

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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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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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

Dosage Form: Tablet

Category: Coating Systems & Additives, Controlled & Modified Release

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

Technical Specifications: Not Available

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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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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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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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LM Application #LearnMore

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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Applications:

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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Applications:

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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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:

Ready-to-use direct compression solution for tablets.

Ingredient(s): Crospovidone, Lactose, Povidone

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression, Granulation

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

Technical Specifications: Not Available

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Applications:

Coating, Moisture Protection

Ingredient(s): HPMC Based Granules

Dosage Form: Granule / Pellet, Powder, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: EXCiPACT

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Applications:

Coating

Ingredient(s): HPMC Based Granules

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives, Coloring Agents

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

Technical Specifications: EXCiPACT

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Applications:

Coating

Ingredient(s): HPMC Based Granules

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives, Coloring Agents

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

Technical Specifications: EXCiPACT

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Applications:

Ready-to-use direct compression solution for lozenges, chewables and effervescent tablets.

Ingredient(s): Lactose, Povidone

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression, Granulation

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

Technical Specifications: Not Available

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Applications:

Coloring Agents

Ingredient(s): HPMC Based Granules

Dosage Form: Tablet

Category: Coating Systems & Additives

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

Technical Specifications: EXCiPACT

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Applications:

Coating

Ingredient(s): HPMC Based Granules

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: EXCiPACT

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Applications:

Coating, Core-Sealing

Ingredient(s): Shellac Based Granules

Dosage Form: Granule / Pellet, Tablet

Category: Coating Systems & Additives

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

Technical Specifications: EXCiPACT

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Applications:

Coating

Ingredient(s): HPMC & Sugar Based Granules

Dosage Form: Tablet

Category: Coating Systems & Additives

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

Technical Specifications: EXCiPACT

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Applications:

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

Ingredient(s): Polyethelyne Glycol 1000

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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Applications:

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

Ingredient(s): Polyethylene Glycol 1450

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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Applications:

Capsule Filling, Direct Compression, Binding, Disintegration

Ingredient(s): Native & Pregelatinized Corn Starch

Dosage Form: Granule / Pellet, Tablet

Category: Direct Compression

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

Technical Specifications: EXCiPACT

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Applications:

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

Ingredient(s): Povidone

Dosage Form: Capsule, Tablet, Transdermal Patch

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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KOLLIDON 30 LP

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Applications:

Binder for peroxide sensitive drugs in solid oral dosage forms. Drug solubilizer with low peroxide in transdermal patches.

Ingredient(s): Povidone

Dosage Form: Capsule, Granule / Pellet, Tablet

Category: Fillers, Diluents & Binders, Granulation

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

Technical Specifications: Not Available

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Applications:

Maximum disintegration

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Capsule, Granule / Pellet, Tablet

Category: Direct Compression, Disintegrants & Superdisintegrants

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

Technical Specifications: Not Available

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Applications:

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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Applications:

Solubility and bioavailability enhancement, ideal for hot melt extrusion (HME)

Ingredient(s): polyethylene glycol, Polyvinyl Acetate

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

Category: Controlled & Modified Release, Granulation, Solubilizers

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Polyvinyl caprolactam – polyvinyl acetate – polyethylene glycol graft copolymer

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Crospovidone, Mannitol, Polyvinyl Acetate

Dosage Form: Orodispersible Tablet

Category: Chewable & Orodispersible Aids, Direct Compression, Granulation

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: 90 % mannitol, 5 % crospovidone, 5 % polyvinyl acetate

Technical Specifications: Not Available

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Applications:

Hydrophilic fill for solubilization of hydrophilic APIs.

Ingredient(s): Polyethylene Glycol 600

Dosage Form: Softgel Capsule

Category: Solubilizers

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

Technical Specifications: Not Available

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Applications:

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

Ingredient(s): Corn Starch, Lactose

Dosage Form: Capsule, Tablet

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

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

Technical Specifications: Not Available

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