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 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

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 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

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

Fi Europe

Attending

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

SPI Pharma

U.S.A

CPhI India

Booth #8.Q31

SPI Pharma has been solving formulation challenges using superior functional materials.

Dosage Form : Tablet

Grade : Oral

Brand Name : Advantose FS95

Application : Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Taste Masking

Excipient Details : Advantose® FS95 is spray-dried fructose coprocessed with starch, is a highly compressible pharmaceutical excipient with chewable vitamin applications.

Pharmacopoeia Ref : NA

Technical Specs : NA

Ingredient(s) : Fructose, Starch

Dosage Form : Tablet

Grade : Oral

SPI Pharma has been solving formulation challenges using superior functional materials.

Ingredient(s) : Fructose, Starch

Dosage Form : Tablet

Category : Chewable & Orodispersible Aids, Co-Processed Excipients, Direct Compression, Taste Masking

Brand : ADVANTOSE FS95

Applications : Advantose® FS95 is spray-dried fructose coprocessed with starch, is a highly compressible pharmaceutical excipient with chewable vitamin applications.

Pharmacopoeia Ref : NA

Technical Specs : NA

Grade : Oral

07

SPI Pharma

U.S.A

CPhI India

Booth #8.Q31

SPI Pharma has been solving formulation challenges using superior functional materials.

Dosage Form : Orodispersible Tablet, Tablet

Grade : Oral

Brand Name : MS90

Application : Chewable & Orodispersible Aids, Direct Compression, Taste Masking

Excipient Details : MS90 is a directly compressible magnesium hydroxide with starch used for chewable tablets due to its smooth mouthfeel and creamy texture.

Pharmacopoeia Ref : NA

Technical Specs : PSD D50: 150-170 µm, Tapped Density: 0.80

Ingredient(s) : Magnesium Hydroxide Excipient, Starch

Dosage Form : Orodispersible Tablet, Tablet

Grade : Oral

SPI Pharma has been solving formulation challenges using superior functional materials.

Ingredient(s) : Magnesium Hydroxide Excipient, Starch

Dosage Form : Orodispersible Tablet, Tablet

Category : Chewable & Orodispersible Aids, Direct Compression, Taste Masking

Brand : MS90

Applications : MS90 is a directly compressible magnesium hydroxide with starch used for chewable tablets due to its smooth mouthfeel and creamy texture.

Pharmacopoeia Ref : NA

Technical Specs : PSD D50: 150-170 µm, Tapped Density: 0.80

Grade : Oral

08

SPI Pharma

U.S.A

CPhI India

Booth #8.Q31

SPI Pharma has been solving formulation challenges using superior functional materials.

Dosage Form : Capsule, Granule / Pellet, Tablet

Grade : Oral

Brand Name : TAP®

Application : Solubilizers

Excipient Details : TAP® pellets are spherical cores made of tartaric acid used for solubility enhancement of drugs exhibiting poor solubility in alkali environments.

Pharmacopoeia Ref : NA

Technical Specs : Bulk density: 0.8-1.1 g/ml

Ingredient(s) : Tartaric Acid

Dosage Form : Capsule, Granule / Pellet, Tablet

Grade : Oral

SPI Pharma has been solving formulation challenges using superior functional materials.

Ingredient(s) : Tartaric Acid

Dosage Form : Capsule, Granule / Pellet, Tablet

Category : Solubilizers

Brand : TAP®

Applications : TAP® pellets are spherical cores made of tartaric acid used for solubility enhancement of drugs exhibiting poor solubility in alkali environments.

Pharmacopoeia Ref : NA

Technical Specs : Bulk density: 0.8-1.1 g/ml

Grade : Oral

09

DKSH

Switzerland

CPhI India

Booth #8.R08

DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.

Dosage Form : Capsule, Solution, Syrup, Tablet

Grade : Oral

Brand Name : HDK® N20 PHARMA

Application : Emulsifying Agents

Excipient Details : HDK N20 Pharma is used as a pharmaceutical emulsifying agent in tablets, capsules, syrups, and solutions.

Pharmacopoeia Ref : GRAS certificate, GMP

Technical Specs : N/A

Ingredient(s) : Silicon Dioxide

Dosage Form : Capsule, Solution, Syrup, Tablet

Grade : Oral

DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.

Ingredient(s) : Silicon Dioxide

Dosage Form : Capsule, Solution, Syrup, Tablet

Category : Emulsifying Agents

Brand : HDK® N20 PHARMA

Applications : HDK N20 Pharma is used as a pharmaceutical emulsifying agent in tablets, capsules, syrups, and solutions.

Pharmacopoeia Ref : GRAS certificate, GMP

Technical Specs : N/A

Grade : Oral

10

DKSH

Switzerland

CPhI India

Booth #8.R08

DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.

Dosage Form : Suspension

Grade : Oral

Brand Name : Sodium Alginate

Application : Rheology Modifiers, Thickeners and Stabilizers

Excipient Details : Sodium Alginate is used as a thickening agent and viscosity modifier in oral liquids such as suspensions.

Pharmacopoeia Ref : N/A

Technical Specs : N/A

Ingredient(s) : Sodium Alginate Excipient

Dosage Form : Suspension

Grade : Oral

DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.

Ingredient(s) : Sodium Alginate Excipient

Dosage Form : Suspension

Category : Rheology Modifiers, Thickeners and Stabilizers

Brand : SODIUM ALGINATE

Applications : Sodium Alginate is used as a thickening agent and viscosity modifier in oral liquids such as suspensions.

Pharmacopoeia Ref : N/A

Technical Specs : N/A

Grade : Oral

Looking for Diclofenac Sodium? Find Diclofenac Sodium based excipient solutions to address drug delivery challenges on PharmaCompass.

Diclofenac Sodium

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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

47 Drugs in Development

FINISHED DOSAGE FORMULATIONS

670 FDF Dossiers

100 FDA Orange Book

277 Europe

34 Canada

62 South Africa

197 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