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Looking for API Stability Enhancers? Find Capsule Dosage Form manufacturers & suppliers on PharmaCompass.

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Anhui Sunhere Pharmaceutical Excipients Co.,Ltd

BASF

Beneo

Capsugel

Corel Pharma Chem

DFE Pharma

Finar

Gangwal Chemicals

Kerry

Kima Chemical

Microlex e.U

Minakem

Nanjing Bold Chemical

PMC Isochem

Pfanstiehl

Rochem International Inc

Roquette

Seppic

Shanghai Shenmei Pharmaceutical Technology Co., Ltd

Shanghai Welltone Material Technology Co., Ltd

Shijiazhuang Huaxu Pharmaceutical

The Dow Chemical Company

Vasa Pharmachem

Vertellus

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Applications: Vitamin E TPGS (Tocophersolan) is a multirole excipient for pharmaceutical drug delivery. It can be used as a solubilizer for poorly soluble drugs and as an emulsifying agent, plasticizer, stabilizer & vehicle for lipid based formulations.

Ingredient(s): Tocophersolan

Dosage Form: Capsule

Category: Film Formers & Plasticizers, Solubilizers

Route of Administration (Grade): Oral, Parenteral, Nasal, Ophthalmic, Topical
Pharmacopoeia Reference: USP 40 – NF 35

Technical Specifications: Specific Gravity: 1.06 at 50°C to 1.03 at 90°C; Solubility In Water: -20% at 20°C; Viscosity: 390cP at 50°C

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Applications: Propyl Gallate, is an ester formed from gallic acid & propanol and is used as an antioxidant. It is used in the oral solids, mostly aimed at modulating the stability of APIs. They are used to improve the shelf life of pharmaceuticals.

Ingredient(s): Propyl Gallate

Dosage Form: Capsule

Category: API Stability Enhancers

Route of Administration (Grade): Oral, Topical
Pharmacopoeia Reference: USP, EP, ICH, Q7GMP

Technical Specifications: NA

Virtual BoothGlobal Pharmaceutical Dosage Solutions Company

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Applications: DRcaps® are made with an innovative HPMC formulation that can help protect sensitive ingredients from the low pH environment of the stomach. The low-moisture level of DRcaps® provides enhanced stability for hygroscopic ingredients.

Ingredient(s): Hydroxypropyl Methyl Cellulose

Dosage Form: Capsule

Category: API Stability Enhancers, Taste Masking, Vegetarian Capsules

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

Technical Specifications: Size # 0-1

Virtual BoothGlobal Pharmaceutical Dosage Solutions Company

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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: Mannitol is mainly used as a bulking agent in tableting. It is also used as taste masking agent in ODT formulations.

Ingredient(s): Mannitol

Dosage Form: Capsule

Category: Fillers, Diluents & Binders

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

Technical Specifications: Not Available

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Applications: Orally Disintegrating Tablets,Sachets, Dispersible Tablets, Sachets, Chewable Tablets, Sublingual Tablets

Ingredient(s): Crospovidone, Dibasic Calcium Phosphate, Mannitol, Microcrystalline Cellulose, Xylitol Excipient

Dosage Form: Capsule

Category: Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Taste Masking

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Japanese Pharmaceutical Excipients. All components meet USP-NF, JP, EP. US DMF Type IV filed.

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

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: Sodium Stearyl Fumarate is used as a lubricant pharmaceutical solid dosage forms to reduce the friction and the adhesion. They also give the tablet strength and disintegration.

Ingredient(s): Sodium Stearyl Fumarate

Dosage Form: Capsule

Category: Lubricants & Glidants

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP, EP, ICH, Q7GMP

Technical Specifications: NA

Virtual BoothGlobal Pharmaceutical Dosage Solutions Company

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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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Ingredient(s): Tyloxapol Excipient

Dosage Form: Capsule

Category: Surfactant & Foaming Agents

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

Technical Specifications: Not Available

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Applications: Film Forming Agent, Wet/Dry Granulation- Binder,Thickening & Suspension Agent, Non-Gelatin Capsule Manufacturing & Enteric Film Coating Systems

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Capsule

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: Primojel® is a superdisintegrant suitable for a variety of tablet & capsule formulations. In higher concentrations, It can act as a dissolution enhancing agent.

Ingredient(s): Sodium Starch Glycolate

Dosage Form: Capsule

Category: Disintegrants & Superdisintegrants

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

Technical Specifications: Not Available

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Applications: Polysorbate 80 in dry powder form, a solubilizing agent acts as a surfactant and increases the solubility of various oral dosage forms.

Ingredient(s): Magnesium aluminium silicate, Polysorbate 80

Dosage Form: Capsule

Category: API Stability Enhancers, Direct Compression, Solubilizers

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

Technical Specifications: Solubilizer in powder form, used in directly compressible dosage forms, Wet granulation, added during lubrication stage

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Applications: Ready mix Non-Functional film coating system.

Ingredient(s): Hydroxypropyl Methyl Cellulose, polyethylene glycol, Talc Excipient

Dosage Form: Capsule

Category: Coating Systems & Additives, Film Formers & Plasticizers

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP, EP, JP; Having US-DMF

Technical Specifications: Not Available