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01 2Minakem
02 13Evonik
03 5Rochem International Inc
04 9SPI Pharma
05 40DKSH
06 6Boai NKY Pharmaceuticals Ltd
07 8Gangwal Healthcare
08 30Nanjing Well Pharmaceutical
09 1Shanghai Minbiotech
10 1Pfanstiehl
11 3Kirsch Pharma
12 4ACG Worldwide
13 22Actylis
14 2Aeon Procare
15 3Alcedo Pharmachem
16 14Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
17 3Ashland
18 110BASF
19 3CD Formulation
20 2Clariant
21 31Corel Pharma Chem
22 7DFE Pharma
23 1Esteem Industries
24 6Finar
25 25Gangwal Chemicals
26 12Ideal Cures
27 3Ingredion Pharma Solutions
28 27Kerry
29 3Keval Exports
30 8Kima Chemical
31 6Lonza Capsugel
32 22Microlex e.U
33 7Nanjing Bold Chemical
34 3Nitika Pharmaceutical Specialities
35 2Nomisma Healthcare
36 6Novo Excipients
37 7Pharmatrans-Sanaq
38 11Pluviaendo
39 5Prachin Chemical
40 1Qianhao Chemical (Hebei) Co., Ltd
41 3Qualicaps
42 59Roquette
43 39Seppic
44 12Shanghai Shenmei Pharmaceutical Technology Co., Ltd
45 13Sigachi Industries
46 4Silverline Chemicals
47 7The Dow Chemical Company
48 2Ulanqab Kema New Material
49 6Valens Pharmachem
50 7Vasa Pharmachem
51 6Vertellus
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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
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, Cream / Lotion / Ointment, Emulsion, Suspension, Tablet
Grade : Topical, Oral
Brand Name : Carboxymethyl Cellulose
Application : Coating Systems & Additives, Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Thickeners and Stabilizers
Excipient Details : Carboxymethylcellulose serves as a disintegrant, binder, coating agent & thickener in oral formulations, also as a stabilizer in topical formulations.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Carboxymethyl Cellulose Sodium
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Suspension, Tablet
Grade : Topical, Oral
Ingredient(s) : Carboxymethyl Cellulose Sodium
Dosage Form : Capsule, Cream / Lotion / Ointment, Emulsion, Suspension, Tablet
Category : Coating Systems & Additives, Disintegrants & Superdisintegrants, Fillers, Diluents & Binders, Thickeners and Stabilizers
Brand : CARBOXYMETHYL CELLULOSE
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
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
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