01

EUROAPI

France

DDL Conference

Attending

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

Dosage Form : Cream / Lotion / Ointment, Injectable / Parenteral

Grade : Topical, Parenteral

Brand Name : Purified Glycerin

Application : Parenteral, Topical

Excipient Details : Purified glycerin is used in topical dosage forms such as creams, lotions, and ointments. It is also used as a solvent in parenteral formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Ingredient(s) : Glycerol Excipient

Dosage Form : Cream / Lotion / Ointment, Injectable / Parenteral

Grade : Topical, Parenteral

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

Ingredient(s) : Glycerol Excipient

Dosage Form : Cream / Lotion / Ointment, Injectable / Parenteral

Category : Parenteral, Topical

Brand : PURIFIED GLYCERIN

Applications : Purified glycerin is used in topical dosage forms such as creams, lotions, and ointments. It is also used as a solvent in parenteral formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Grade : Topical, Parenteral

02

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Dosage Form : Capsule, Tablet

Grade : Oral

Brand Name : EUDRAGIT® L 12,5

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

Dosage Form : Capsule, Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer

Dosage Form : Capsule, Tablet

Category : Solubilizers

Brand : EUDRAGIT® L 12,5

Applications : 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

Grade : Oral

03

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Dosage Form : Capsule, Tablet

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

Dosage Form : Capsule, Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer

Dosage Form : Capsule, Tablet

Category : Coating Systems & Additives, Film Formers & Plasticizers

Brand : EUDRAGIT® L 30 D-55

Applications : 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

Grade : Oral

04

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Dosage Form : Capsule, Tablet

Grade : Oral

Brand Name : EUDRAGIT® FS 30 D

Application : Solubilizers

Excipient Details : EUDRAGIT® FS 30 D (aqueous dispersion), a delayed release polymer, used to increase solubility of poorly soluble OSDs such as tablets and capsules.

Pharmacopoeia Ref : NA

Technical Specs : NA

Ingredient(s) : Methacrylic Acid Excipient, Methyl Acrylate, Methyl Methacrylate

Dosage Form : Capsule, Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Methacrylic Acid Excipient, Methyl Acrylate, Methyl Methacrylate

Dosage Form : Capsule, Tablet

Category : Solubilizers

Brand : EUDRAGIT® FS 30 D

Applications : EUDRAGIT® FS 30 D (aqueous dispersion), a delayed release polymer, used to increase solubility of poorly soluble OSDs such as tablets and capsules.

Pharmacopoeia Ref : NA

Technical Specs : NA

Grade : Oral

05

Rochem International Inc

U.S.A

AIChE Annual Meeting

Not Confirmed

Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

Dosage Form : Cream / Lotion / Ointment, Emulsion, Gel, Solution, Tablet

Grade : Topical, Oral

Brand Name : Gum Arabic

Application : API Stability Enhancers, Emulsifying Agents, Fillers, Diluents & Binders

Excipient Details : Acacia, also known as gum arabic, is used in the pharmaceutical industry as an emulsifier, stabilizing agent, & tablet binder in various formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Ingredient(s) : Gum Arabic

Dosage Form : Cream / Lotion / Ointment, Emulsion, Gel, Solution, Tablet

Grade : Topical, Oral

Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

Ingredient(s) : Gum Arabic

Dosage Form : Cream / Lotion / Ointment, Emulsion, Gel, Solution, Tablet

Category : API Stability Enhancers, Emulsifying Agents, Fillers, Diluents & Binders

Brand : GUM ARABIC

Applications : Acacia, also known as gum arabic, is used in the pharmaceutical industry as an emulsifier, stabilizing agent, & tablet binder in various formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Grade : Topical, Oral

06

EUROAPI

France

DDL Conference

Attending

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

Dosage Form : Tablet

Grade : Oral

Brand Name : Calcium Lactate-Glycerol Ad...

Application : Fillers, Diluents & Binders

Excipient Details : Calcium lactate-glycerol adduct is used both as a stabilizer and a binder in tablet formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Ingredient(s) : Calcium Lactate, Glycerol Excipient

Dosage Form : Tablet

Grade : Oral

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

Ingredient(s) : Calcium Lactate, Glycerol Excipient

Dosage Form : Tablet

Category : Fillers, Diluents & Binders

Brand : CALCIUM LACTATE-GLYCEROL ADDUCT

Applications : Calcium lactate-glycerol adduct is used both as a stabilizer and a binder in tablet formulations.

Pharmacopoeia Ref : NA

Technical Specs : NA

Grade : Oral

07

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Dosage Form : Capsule, Tablet

Grade : Oral

Brand Name : EUDRAGIT® S 12,5

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

Dosage Form : Capsule, Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer

Dosage Form : Capsule, Tablet

Category : Solubilizers

Brand : EUDRAGIT® S 12,5

Applications : 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

Grade : Oral

08

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

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 and Methyl Methacrylate Copolymer, Methacrylic Acid Excipient

Dosage Form : Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Ethyl Acrylate and Methyl Methacrylate Copolymer, Methacrylic Acid Excipient

Dosage Form : Tablet

Category : Controlled & Modified Release

Brand : EUDRAGIT® RS 12,5

Applications : 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

Grade : Oral

09

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Dosage Form : Capsule, Tablet

Grade : Oral

Brand Name : EUDRAGIT® L 100

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

Dosage Form : Capsule, Tablet

Grade : Oral

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

Ingredient(s) : Methacrylic Acid Methyl Methacrylate Copolymer

Dosage Form : Capsule, Tablet

Category : Controlled & Modified Release, Solubilizers

Brand : EUDRAGIT® L 100

Applications : 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

Grade : Oral

10

Evonik

Germany

CPhI India

Booth #6.M14

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

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

Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

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

Applications : 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

Grade : Oral

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CHEMISTRY

Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

111 API Suppliers

21 USDMF

17 CEP/COS

13 JDMF

9 EU WC

22 KDMF

31 NDC API

45 Listed Suppliers

$ API Reference Price

DEVELOPMENTS

12 Drugs in Development

FINISHED DOSAGE FORMULATIONS

601 FDF Dossiers

100 FDA Orange Book

207 Europe

34 Canada

62 South Africa

198 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET, EXTENDED RELEASE;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

SOLUTION;TOPICAL - 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET, DELAYED RELEASE;ORAL - 50MG;0.2MG

TABLET, DELAYED RELEASE;ORAL - 75MG;0.2MG

SOLUTION;TOPICAL - 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

GEL;TOPICAL - 3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

GEL;TOPICAL - 1%

SOLUTION;INTRAVENOUS - 37.5MG/ML (37.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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TABLET, EXTENDED RELEASE;ORAL - 100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

SOLUTION;TOPICAL - 2% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

SOLUTION;TOPICAL - 1.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

GEL;TOPICAL - 3% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

SOLUTION;INTRAVENOUS - 37.5MG/ML (37.5MG/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons