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Brand Name : Sodium Stearyl Fumarate GMP
Application : Lubricants & Glidants
Excipient Details : Sodium Stearyl Fumarate is used as a lubricant in OSDs to reduce the friction and the adhesion. It also provides tablet strength & disintegration.
Pharmacopoeia Ref : USP, EP, ICH, Q7GMP
Technical Specs : NA
Ingredient(s) : Sodium Stearyl Fumarate
Ingredient(s) : Sodium Stearyl Fumarate
Category : Lubricants & Glidants
Brand : SODIUM STEARYL FUMARATE GMP
Pharmacopoeia Ref : USP, EP, ICH, Q7GMP
Technical Specs : NA
Grade : Oral
Application : Controlled & Modified Release, Solubilizers
Excipient Details : EUDRAGIT® L 100 (powder), a delayed release polymer is used to increase solubility of poorly soluble products such as tablets, capsules, ODTs, etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Category : Controlled & Modified Release, Solubilizers
Brand : EUDRAGIT® L 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Capsule, Liquid, Suspension, Tablet
Grade : Oral
Application : Taste Masking
Excipient Details : Sucralose is a nonnutritive, zero-calorie sweetener, used as taste masking agent in various formulations such as tablets, capsules & suspensions.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Sucralose
Dosage Form : Capsule, Liquid, Suspension, Tablet
Grade : Oral
Ingredient(s) : Sucralose
Dosage Form : Capsule, Liquid, Suspension, Tablet
Category : Taste Masking
Brand : SUCRALOSE
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Taste Masking
Excipient Details : Advantose® FS95 is spray-dried fructose coprocessed with starch, is a highly compressible pharmaceutical excipient with chewable vitamin applications.
Dosage Form : Tablet
Category : Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Taste Masking
Brand : ADVANTOSE FS95
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Capsule, Granule / Pellet, Tablet
Grade : Oral
Brand Name : EUDRAGIT® L 100-55
Application : Coating Systems & Additives, Controlled & Modified Release, Solubilizers
Excipient Details : EUDRAGIT® L 100-55 (powder) is used in delayed release coatings to enhance solubility of poorly soluble drugs such as tablets, capsules & granules.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form : Capsule, Granule / Pellet, Tablet
Grade : Oral
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form : Capsule, Granule / Pellet, Tablet
Category : Coating Systems & Additives, Controlled & Modified Release, Solubilizers
Brand : EUDRAGIT® L 100-55
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Application : Solubilizers
Excipient Details : EUDRAGIT® L 12,5 (organic solution), a delayed release polymer is used to increase solubility of poorly soluble products such as tablets and capsules.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Category : Solubilizers
Brand : EUDRAGIT® L 12,5
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Application : Solubilizers
Excipient Details : EUDRAGIT® S 12,5 (Organic solution) a delayed release polymer, used to increase solubility of poorly soluble drugs such as tablets and capsules.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer
Category : Solubilizers
Brand : EUDRAGIT® S 12,5
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® S 100, a delayed release polymer can be combined with other polymers for precise targeting and rapid drug release in tablets, capsules, etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer 1:2
Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer 1:2
Category : Controlled & Modified Release
Brand : EUDRAGIT® S 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Coating Systems & Additives, Controlled & Modified Release
Excipient Details : ACTILLETS are microcrystalline cellulose spheres developed using advanced drug delivery technology to enable effective loading & coating of particles.
Pharmacopoeia Ref : NA
Technical Specs :
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Tablet
Category : Coating Systems & Additives, Controlled & Modified Release
Brand : ACTILLETS™
Pharmacopoeia Ref : NA
Technical Specs : Not Available
Grade : Oral
Brand Name : EUDRAGIT® L 30 D-55
Application : Coating Systems & Additives, Film Formers & Plasticizers
Excipient Details : EUDRAGIT® L 30 D-55 (aqueous dispersion) is a delayed release polymer used as coating and film former in tablets, capsules, granules etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Category : Coating Systems & Additives, Film Formers & Plasticizers
Brand : EUDRAGIT® L 30 D-55
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral