Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Acetone Excipient
02 1Acetyl Triethyl Citrate
03 1Acetyl tri-n-butyl citrate
04 1Acrylate copolymer
05 1Amino Methacrylate Copolymer
06 3Ammonia Methacrylate Copolymer Type A
07 1Ammonio Methacrylate Copolymer
08 1Ammonio Methacrylate Copolymer Excipient
09 4Ammonio Methacrylate Copolymer Type B
10 1Carbomer 941
11 4Carbomer Homopolymer Type A
12 1Carbomer Homopolymer Type B
13 1Copovidone K25-31
14 1Dibutyl Sebacate
15 5Ethyl Acrylate Methyl Methacrylate Copolymer
16 1Ethyl Cellulose
17 3EthylCellulose
18 1HPMC 2910
19 2Hydrogenated Castor Oil
20 1Hydroxypropyl Betacyclodextrin
21 1Hydroxypropyl Methyl Cellulose
22 9Hydroxypropyl Methylcellulose
23 1Kaolin Excipient
24 1Lauryl Sulfate
25 1METHACRYLIC ACID COPOLYMER TYPE A
26 3Methacrylic Acid & Ethyl Acrylate Copolymer
27 5Methacrylic Acid - Ethyl Acrylate Copolymer
28 1Methacrylic Acid Copolymer Type B
29 2Methacrylic Acid Methyl Methacrylate Copolymer
30 3Microcrystalline Cellulose
31 1PLASACRYL HTP20
32 1PLASACRYL T20
33 2Phenylethyl Alcohol Excipient
34 1Poly DL Lactide
35 1Poly DL Lactide co Glycolide
36 2Poly L Lactide
37 1Poly-DL-Lactic-co-Glycolic Acid
38 1Polycarbophil
39 1Polydextrose Sugar
40 1Polyethylene Oxide
41 1Polyvinyl Acetate
42 3Polyvinyl Alcohol
43 1Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer
44 1Potassium Chloride Excipient
45 2Povidone
46 1Sodium Alginate Excipient
47 2Sodium Citrate Dihydrate Excipient
48 1Sodium Hydroxide Excipient
49 1Starch
50 1Talc Excipient
51 1Tri-n-butyl Citrate
52 1Triethyl Citrate
53 1Xylitol Excipient
54 1hydroxypropyl methylcellulose phthalate
55 2polyethylene glycol
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® E 100 (granules) is an immediate-release polymer used as a taste masking, coating agent & film former in tablets, capsules, powders & ODTs.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Amino Methacrylate Copolymer
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Amino Methacrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® E 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral, Parenteral
Application : Controlled & Modified Release
Excipient Details : Complexol-HP (Hydroxypropyl Betacyclodextrin) is used as stabilizer, solubilizer & taste masking agent in solids, liquids, ophthalmics & injectables.
Pharmacopoeia Ref : BP/EP/USP-NF
Technical Specs : NA
Ingredient(s) : Hydroxypropyl Betacyclodextrin
Dosage Form : Tablet
Grade : Oral, Parenteral
Ingredient(s) : Hydroxypropyl Betacyclodextrin
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : COMPLEXOL HP®
Pharmacopoeia Ref : BP/EP/USP-NF
Technical Specs : NA
Grade : Oral, Parenteral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
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 COPOLYMER TYPE A
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : METHACRYLIC ACID COPOLYMER TYPE A
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® L 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : DiCOM-DC SR300 is used as a directly compressible, rate-controlling, and co-processed excipient in sustained-release tablets and capsules.
Pharmacopoeia Ref : In-house
Technical Specs : NA
Ingredient(s) : EthylCellulose, Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose, Magnesium Stearate, Maize Starch, Microcrystalline Cellulose, Silicon Dioxide, Talc
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : EthylCellulose, Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose, Magnesium Stearate, Maize Starch, Microcrystalline Cellulose, Silicon Dioxide, Talc
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : DICOM-DC® SR300
Pharmacopoeia Ref : In-house
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® L 100-55
Application : Controlled & Modified Release
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 : Tablet
Grade : Oral
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® L 100-55
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RL 100 (granules) is an excipient used as a solubilizer in combination with Eudragit® RS for creating sustained release drugs.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ammonia Methacrylate Copolymer Type A
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ammonia Methacrylate Copolymer Type A
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RL 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS, a functional sustained release polymer, used in combination with EUDRAGIT® RL for customized release profiles in tablets, capsules, etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ammonio Methacrylate Copolymer Type B
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ammonio Methacrylate Copolymer Type B
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RS 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
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 Copolymer Type B
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Methacrylic Acid Copolymer Type B
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® S 100
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : PlasACRYL HTP20 is an easy-to-use glidant & plasticizer premix, specifically designed for EUDRAGIT® L 30 D-55 products such as capsules, tablets, etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : PLASACRYL HTP20
Dosage Form : Tablet
Grade : Oral
Brand : PLASACRYL® HTP20
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : PlasACRYL® T20 is an easy-to-use glidant & plasticizer premix, specifically designed for EUDRAGIT® FS 30 D products such as capsules, tablets, etc.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : PLASACRYL T20
Dosage Form : Tablet
Grade : Oral
Brand : PLASACRYL® T20
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RL 30 D
Application : Controlled & Modified Release
Excipient Details : Eudragit RL 30 D(aqueous dispersion) is a sustained release polymer for customized release profiles, used in combination with EUDRAGIT® RS.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RL 30 D
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS PO (Powder) is an insoluble sustained release polymer for customized release profiles used in combination with EUDRAGIT® RL.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ammonio Methacrylate Copolymer Excipient
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ammonio Methacrylate Copolymer Excipient
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RS PO
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : Gellets-P are Microcrystalline Cellulose based spheres for the manufacturing of pellets and modified release products.
Pharmacopoeia Ref : In-house
Technical Specs : NA
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : GELLETS-P®
Applications : Gellets-P are Microcrystalline Cellulose based spheres for the manufacturing of pellets and modified release products.
Pharmacopoeia Ref : In-house
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RS 30 D
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS 30 D(aqueous dispersion) is a sustained release polymer for customized release profiles used in combination with EUDRAGIT® RL.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RS 30 D
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® RS 12,5
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RS 12,5 (Organic solution) is a sustained release polymer for customized release profiles used in combination with EUDRAGIT® RL.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer, Methacrylic Acid Excipient
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer, Methacrylic Acid Excipient
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® RS 12,5
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® NE 30 D
Application : Controlled & Modified Release
Excipient Details : Eudragit NE 30 D (aqueous dispersion) is a highly flexible sustained release polymer used for coating (without plasticizer) in OSDs.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® NE 30 D
Applications : Eudragit NE 30 D (aqueous dispersion) is a highly flexible sustained release polymer used for coating (without plasticizer) in OSDs.
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Brand Name : EUDRAGIT® NE 40 D
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® NE 40 D (aqueous dispersion) is a sustained release polymer used for coating tablets, granules and pellets.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Grade : Oral
Ingredient(s) : Ethyl Acrylate Methyl Methacrylate Copolymer
Dosage Form : Tablet
Category : Controlled & Modified Release
Brand : EUDRAGIT® NE 40 D
Applications : EUDRAGIT® NE 40 D (aqueous dispersion) is a sustained release polymer used for coating tablets, granules and pellets.
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral