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Looking for Tox21_300015? Find Controlled & Modified Release used in Tox21_300015 to address drug delivery challenges on PharmaCompass.

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01 Capsule (8)

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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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ACETONE NF

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Applications:

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

Ingredient(s): Acetone Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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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, Tablet

Category: Controlled & Modified Release

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

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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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, Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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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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SODIUM CITRATE DIHYDRATE MULTI-COMPENDIAL

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Applications:

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

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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SODIUM CITRATE DIHYDRATE USP-NF

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Applications:

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

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Capsule, Tablet

Category: Controlled & Modified Release

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

Technical Specifications: Not Available

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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:

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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