Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 7Evonik
02 1Faran Shimi Pharmaceutical
03 5Gangwal Healthcare
04 5Nanjing Well Pharmaceutical
05 2Actylis
06 2Aeon Procare
07 3Alcedo Pharmachem
08 36BASF
09 3Corel Pharma Chem
10 7Finar
11 2Gangwal Chemicals
12 7Ideal Cures Pvt Ltd
13 18Kerry
14 1Kima Chemical
15 1Lonza Capsugel
16 2Nomisma Healthcare
17 2Pluviaendo
18 1Sigachi Industries
19 5The Dow Chemical Company
20 3Vertellus
Application : Controlled & Modified Release, Solubilizers
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
Ingredient(s) : METHACRYLIC ACID COPOLYMER TYPE A
Category : Controlled & Modified Release, Solubilizers
Brand : EUDRAGIT® L 100
Pharmacopoeia Ref : NA
Technical Specs : Available as powder; Other grades- EUDRAGIT® L 12,5
Grade : Oral
Dosage Form : Injectable / Parenteral
Grade : Parenteral
Brand Name : Potassium Chloride
Application : Parenteral
Excipient Details : Potassium chloride is used as a diuretic-osmotic in injectable and parenteral solutions.
Pharmacopoeia Ref : NA
Technical Specs : NA
Ingredient(s) : Potassium Chloride Excipient
Dosage Form : Injectable / Parenteral
Grade : Parenteral
Ingredient(s) : Potassium Chloride Excipient
Dosage Form : Injectable / Parenteral
Category : Parenteral
Brand : POTASSIUM CHLORIDE
Applications : Potassium chloride is used as a diuretic-osmotic in injectable and parenteral solutions.
Pharmacopoeia Ref : NA
Technical Specs : NA
Grade : Parenteral
Application : Co-Processed Excipients, Controlled & Modified Release, Direct Compression
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
Brand : DICOM-DC® SR300
Pharmacopoeia Ref : In-house
Technical Specs : NA
Grade : Oral
Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels
Grade : Parenteral, Topical, Oral
Brand Name : Polyethylene Glycol 400
Application : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Excipient Details : PEG 400 is used as a suspending agent, stabilizer, plasticizer and filler in OSDs, liquids & semi-solids and as a solvent for parenteral formulations.
Pharmacopoeia Ref : ChP/USP/EP
Technical Specs : NA
Ingredient(s) : Polyethylene Glycol 400
Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels
Grade : Parenteral, Topical, Oral
Ingredient(s) : Polyethylene Glycol 400
Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels
Category : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical
Brand : POLYETHYLENE GLYCOL 400
Pharmacopoeia Ref : ChP/USP/EP
Technical Specs : NA
Grade : Parenteral, Topical, Oral
Dosage Form : Capsule, Granule / Pellet, Tablet
Grade : Oral
Brand Name : EUDRAGIT® L 100-55
Application : Controlled & Modified Release, Solubilizers
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, Granule / Pellet, Tablet
Grade : Oral
Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form : Capsule, Granule / Pellet, Tablet
Category : Controlled & Modified Release, Solubilizers
Brand : EUDRAGIT® L 100-55
Pharmacopoeia Ref : NA
Technical Specs : Available as powder; Other grades- EUDRAGIT® L 30 D-55
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
Ingredient(s) : Methacrylic Acid Copolymer Type B
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, Granule / Pellet, 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 : Capsule, Granule / Pellet, Tablet
Grade : Oral
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Capsule, Granule / Pellet, 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