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 4Ammonio Methacrylate Copolymer Type B
09 1Carbomer 941
10 4Carbomer Homopolymer Type A
11 1Carbomer Homopolymer Type B
12 1Copovidone K25-31
13 1Dibutyl Sebacate
14 1Ethyl Cellulose
15 3EthylCellulose
16 1HPMC 2910
17 2Hydrogenated Castor Oil
18 1Hydroxypropyl Betacyclodextrin
19 1Hydroxypropyl Methyl Cellulose
20 9Hydroxypropyl Methylcellulose
21 1Kaolin Excipient
22 1Lauryl Sulfate
23 1METHACRYLIC ACID COPOLYMER TYPE A
24 3Methacrylic Acid & Ethyl Acrylate Copolymer
25 5Methacrylic Acid - Ethyl Acrylate Copolymer
26 1Methacrylic Acid Copolymer Type B
27 2Methacrylic Acid Methyl Methacrylate Copolymer
28 3Microcrystalline Cellulose
29 1PLASACRYL HTP20
30 1PLASACRYL T20
31 2Phenylethyl Alcohol Excipient
32 1Poly DL Lactide
33 1Poly DL Lactide co Glycolide
34 2Poly L Lactide
35 1Poly-DL-Lactic-co-Glycolic Acid
36 1Polycarbophil
37 1Polydextrose Sugar
38 1Polyethylene Oxide
39 1Polyvinyl Acetate
40 3Polyvinyl Alcohol
41 1Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer
42 1Potassium Chloride Excipient
43 2Povidone
44 1Sodium Alginate Excipient
45 2Sodium Citrate Dihydrate Excipient
46 1Sodium Hydroxide Excipient
47 1Starch
48 1Talc Excipient
49 1Tri-n-butyl Citrate
50 1Triethyl Citrate
51 1Xylitol Excipient
52 1hydroxypropyl methylcellulose phthalate
53 2polyethylene glycol
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® E is an immediate-release polymer used as a taste masking & coating agent to improve swallowability of tablets, ODTs, capsules, powder, etc.
Pharmacopoeia Ref : NA
Technical Specs : Available as granules; Other grades- EUDRAGIT® E 12,5, EUDRAGIT® E PO.
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 : Available as granules; Other grades- EUDRAGIT® E 12,5, EUDRAGIT® E PO.
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, a functional delayed release polymer is used to increase solubility of poorly soluble products such as tablets, capsules, ODTs, etc.
Pharmacopoeia Ref : NA
Technical Specs : Available as powder; Other grades- EUDRAGIT® L 12,5
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 : Available as powder; Other grades- EUDRAGIT® L 12,5
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 polymer is used in delayed, sustained-release coatings to enhance solubility of poorly soluble drugs such as tablets, capsules, etc.
Pharmacopoeia Ref : NA
Technical Specs : Available as powder; Other grades- EUDRAGIT® L 30 D-55
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 : Available as powder; Other grades- EUDRAGIT® L 30 D-55
Grade : Oral
Dosage Form : Tablet
Grade : Oral
Application : Controlled & Modified Release
Excipient Details : EUDRAGIT® RL, an insoluble, highly permeable polymer used in combination with EUDRAGIT® RS in customized release drugs such as tablets, capsules, etc.
Pharmacopoeia Ref : NA
Technical Specs : Other grades- EUDRAGIT® RL 12,5, EUDRAGIT® RL 30 D, EUDRAGIT® RL PO
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 : Other grades- EUDRAGIT® RL 12,5, EUDRAGIT® RL 30 D, EUDRAGIT® RL PO
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 : Available as granules; Other grades- EUDRAGIT® RS 12,5, EUDRAGIT® RS 30 D, EUDRAGIT® RS PO
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 : Available as granules; Other grades- EUDRAGIT® RS 12,5, EUDRAGIT® RS 30 D, EUDRAGIT® RS PO
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 : Available as powder; Other grades- EUDRAGIT® S 12,5
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 : Available as powder; Other grades- EUDRAGIT® S 12,5
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 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 T20
Dosage Form : Tablet
Grade : Oral
Brand : PLASACRYL® T20
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