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Looking for Capsule? Find Controlled & Modified Release & other pharma excipients for Capsule dosage forms on PharmaCompass.

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01 Acetone Excipient (1)

02 Acetyl Triethyl Citrate (1)

03 Acetyl tri-n-butyl citrate (1)

04 Alginic Acid (1)

05 Amino Methacrylate Copolymer (1)

06 Ammonia Methacrylate Copolymer Type A (1)

07 Ammonio Methacrylate Copolymer Type B (1)

08 Dibutyl Sebacate (1)

09 Ethyl Cellulose (1)

10 EthylCellulose (2)

11 HPMC AS (1)

12 Hydrogenated Castor Oil (1)

13 Hydroxypropyl Methylcellulose (3)

14 Lauryl Sulfate (1)

15 METHACRYLIC ACID COPOLYMER TYPE A (1)

16 Methacrylic Acid & Ethyl Acrylate Copolymer (3)

17 Methacrylic Acid - Ethyl Acrylate Copolymer (3)

18 Methacrylic Acid Copolymer Type B (1)

19 Microcrystalline Cellulose (1)

20 PLASACRYL HTP20 (1)

21 PLASACRYL T20 (1)

22 Phenylethyl Alcohol Excipient (2)

23 Polyvinyl Acetate (1)

24 Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer (1)

25 Potassium Chloride Excipient (1)

26 Povidone (2)

27 Sodium Citrate Dihydrate Excipient (2)

28 Sodium Hydroxide Excipient (1)

29 Talc Excipient (1)

30 Tri-n-butyl Citrate (1)

31 Triethyl Citrate (1)

32 hydroxypropyl methylcellulose phthalate (1)

33 polyethylene glycol (1)

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01 DKSH (2)

02 Evonik (8)

03 Gangwal Healthcare (2)

04 Actylis (6)

05 Alcedo Pharmachem (2)

06 BASF (8)

07 Corel Pharma Chem (1)

08 Finar (2)

09 Gangwal Chemicals (1)

10 Kerry (3)

11 Lonza Capsugel (1)

12 The Dow Chemical Company (2)

13 Vertellus (5)

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01 Germany (16)

02 India (8)

03 Switzerland (2)

04 U.S.A (17)

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Applications:

Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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ACETONE NF

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Applications:

A&C’s Acetone NF meets the USP-NF monograph.

Ingredient(s): Acetone Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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POLYETHYLENE GLYCOL 400 NF

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Ingredient(s): polyethylene glycol

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Controlled Release, Direct Compression,Wet Granulation,Tablet Coating, Liquid Solutions and Suspensions

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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POTASSIUM CHLORIDE

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Ingredient(s): Potassium Chloride Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

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

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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PHENYL ETHYL ALCOHOL MULTI-COMPENDIAL

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Applications:

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

Ingredient(s): Phenylethyl Alcohol Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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DIBUTYL SEBACATE

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Applications:

Controlled-release coatings for tablets & capsules.

Ingredient(s): Dibutyl Sebacate

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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PHENYL ETHYL ALCOHOL USP

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Applications:

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

Ingredient(s): Phenylethyl Alcohol Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

Enteric, Delayed Release Matrix and Solubility Enhancement

Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Methylacryli acid and Ethyl Acrylate copolymer (1:1) Type A

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SODIUM CITRATE DIHYDRATE MULTI-COMPENDIAL

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Applications:

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

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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SODIUM CITRATE DIHYDRATE USP-NF

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Applications:

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

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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SODIUM HYDROXIDE NF

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Applications:

A&C's Sodium Hydroxide is a highly caustic concentrate solution.

Ingredient(s): Sodium Hydroxide Excipient

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Solution 50% (w/w)

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NUTRACOAT EC25D

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Applications:

Sustained Release, Taste Masking, Moisture Barrier, Binder in Wet Granulation

Ingredient(s): Ethyl Cellulose

Dosage Form: Capsule

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF: Ethyl cellulose dispersion Type B

Technical Specifications: Not Available

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Applications:

Enteric coating with release above pH 5.5 (partially preneutralized powder)

Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer

Dosage Form: Capsule

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Methacrylic Acid

Technical Specifications: Not Available

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Applications:

Enteric coating with release above pH 5.5 (30 % solids content dispersion)

Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer

Dosage Form: Capsule

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Methacrylic Acid

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

Category: Controlled & Modified Release

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:

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

Ingredient(s): Povidone

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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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

Category: Controlled & Modified Release

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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Applications:

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

Ingredient(s): Povidone

Dosage Form: Capsule

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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Applications:

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

Category: 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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