SPI Pharma has been solving formulation challenges using superior functional materials.
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01 7SPI Pharma
02 1Gangwal Healthcare
03 13Evonik
04 3Rochem International Inc
05 25DKSH
06 9Nanjing Well Pharmaceutical
07 1Pfanstiehl
08 3Kirsch Pharma
09 1ACG Worldwide
10 12Actylis
11 2Aeon Procare
12 2Alcedo Pharmachem
13 6Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
14 16BASF
15 28Corel Pharma Chem
16 3Finar
17 16Gangwal Chemicals
18 11Ideal Cures
19 2Ingredion Pharma Solutions
20 9Kerry
21 4Kima Chemical
22 6Lonza Capsugel
23 3Microlex e.U
24 4Nanjing Bold Chemical
25 1Novo Excipients
26 4Pluviaendo
27 1Qianhao Chemical (Hebei) Co., Ltd
28 1Qualicaps
29 29Roquette
30 40Seppic
31 4Shanghai Shenmei Pharmaceutical Technology Co., Ltd
32 2Sigachi Industries
33 3The Dow Chemical Company
34 3Valens Pharmachem
35 1Vasa Pharmachem
36 3Vertellus
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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
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 : Cream / Lotion / Ointment, Emulsion, Suspension
Grade : Topical, Oral
Application : Emulsifying Agents, Thickeners and Stabilizers
Excipient Details : Carrageenan is used as an emulsifying, stabilizing & suspending agent in various non-parenteral dosage forms, such as suspensions, emulsions & creams.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Carrageenan
Dosage Form : Cream / Lotion / Ointment, Emulsion, Suspension
Grade : Topical, Oral
Ingredient(s) : Carrageenan
Dosage Form : Cream / Lotion / Ointment, Emulsion, Suspension
Category : Emulsifying Agents, Thickeners and Stabilizers
Brand : CARRAGEENAN
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Topical, 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
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
Dosage Form : Tablet
Grade : Oral
Application : Co-Processed Excipients
Excipient Details : AHMC 0600 is a co-processed aluminum hydroxide and magnesium carbonate powder used in immediate-relief antacid tablet formulation.
Pharmacopoeia Ref : NA
Technical Specs : Apparent Density: 0.30-0.40 (g/mL)
Ingredient(s) : Aluminum Hydroxide Excipient, Magnesium Carbonate Excipient
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Aluminum Hydroxide Excipient, Magnesium Carbonate Excipient
Dosage Form : Tablet
Category : Co-Processed Excipients
Brand : AHMC 0600
Applications : AHMC 0600 is a co-processed aluminum hydroxide and magnesium carbonate powder used in immediate-relief antacid tablet formulation.
Pharmacopoeia Ref : NA
Technical Specs : Apparent Density: 0.30-0.40 (g/mL)
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Co-Processed Excipients
Excipient Details : AHMC 0611 is a co-processed aluminum hydroxide & magnesium carbonate micronized powder used in immediate-relief antacid tablets & liquid suspensions.
Pharmacopoeia Ref : NA
Technical Specs : Tapped NMT: 0.2
Ingredient(s) : Aluminum Hydroxide Excipient, Magnesium Carbonate Excipient
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Aluminum Hydroxide Excipient, Magnesium Carbonate Excipient
Dosage Form : Tablet
Category : Co-Processed Excipients
Brand : AHMC 0611
Pharmacopoeia Ref : NA
Technical Specs : Tapped NMT: 0.2
Grade : Oral