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 1Amino Methacrylate Copolymer
05 1Ammonia Methacrylate Copolymer Type A
06 1Ammonio Methacrylate Copolymer Type B
07 1Dibutyl Sebacate
08 1Ethyl Cellulose
09 2EthylCellulose
10 1HPMC AS
11 1Hydrogenated Castor Oil
12 1Hydroxypropyl Betacyclodextrin
13 3Hydroxypropyl Methylcellulose
14 1Lauryl Sulfate
15 1METHACRYLIC ACID COPOLYMER TYPE A
16 3Methacrylic Acid & Ethyl Acrylate Copolymer
17 3Methacrylic Acid - Ethyl Acrylate Copolymer
18 1Methacrylic Acid Copolymer Type B
19 1Microcrystalline Cellulose
20 1PLASACRYL HTP20
21 1PLASACRYL T20
22 2Phenylethyl Alcohol Excipient
23 1Polyvinyl Acetate
24 1Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer
25 1Potassium Chloride Excipient
26 2Povidone
27 2Sodium Citrate Dihydrate Excipient
28 1Sodium Hydroxide Excipient
29 1Tri-n-butyl Citrate
30 1Triethyl Citrate
31 1hydroxypropyl methylcellulose phthalate
32 1polyethylene glycol
Dosage Form : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Amino Methacrylate Copolymer
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral, Parenteral
Ingredient(s) : Hydroxypropyl Betacyclodextrin
Dosage Form : Capsule
Category : Controlled & Modified Release
Brand : COMPLEXOL HP®
Pharmacopoeia Ref : BP/EP/USP-NF
Technical Specs : NA
Grade : Oral, Parenteral
Dosage Form : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : METHACRYLIC ACID COPOLYMER TYPE A
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : EthylCellulose, Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose, Magnesium Stearate, Maize Starch, Microcrystalline Cellulose, Silicon Dioxide, Talc
Dosage Form : Capsule
Category : Controlled & Modified Release
Brand : DICOM-DC® SR300
Pharmacopoeia Ref : In-house
Technical Specs : NA
Grade : Oral
Dosage Form : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Ammonia Methacrylate Copolymer Type A
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Ammonio Methacrylate Copolymer Type B
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Methacrylic Acid Copolymer Type B
Dosage Form : Capsule
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 : Capsule
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 : Capsule
Grade : Oral
Brand : PLASACRYL® HTP20
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Capsule
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 : Capsule
Grade : Oral
Brand : PLASACRYL® T20
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Oral
Dosage Form : Capsule
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 : Capsule
Grade : Oral
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Capsule
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