Triethyl Citrate | Pharma Excipients | News | Suppliers

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CHEMISTRY

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INACTIVE PHARMA INGREDIENTS

1 Suppliers, 1 USDMF, 2 Listed Suppliers

1 Suppliers
1 USDMF
2 Listed Suppliers

FINISHED DOSAGE FORMULATIONS

305 FDF Dossiers Suppliers, 22 FDA Listed Dossiers

305 FDF Dossiers Suppliers
22 FDA Listed Dossiers

EXCIPIENTS BY APPLICATIONS

2 Film Formers & Plasticizers, 1 Coating Systems & Additives, 1 Controlled & Modified Release, 1 Fillers, Diluents & Binders, 1 Taste Masking, 1 Surfactant & Foaming Agents

2 Film Formers & Plasticizers
1 Coating Systems & Additives
1 Controlled & Modified Release
1 Fillers, Diluents & Binders
1 Taste Masking
1 Surfactant & Foaming Agents

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow

1 DATA COMPILATION #PharmaFlow

MARKET PLACE

4 EXCIPIENTS

4 EXCIPIENTS

REF. STANDARDS & IMPURITIES

1 USP , 1 Others

1 USP
1 Others

Chemistry

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SUPPLIERS

01

Vertellus

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

KY/TN Water Professionals

Not Confirmed

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USDMF

01

Vertellus Performance Materials Inc

U.S.A

KY/TN Water Professionals

Not Confirmed

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FINISHED DOSAGE FORMULATIONS

Upload your portfolio for free, ask us

FDF DOSSIERS SUPPLIERS

01

ABBVIE

U.S.A

KY/TN Water Professionals

Not Confirmed

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PANCRELIPASE (AMYLASE; LIPASE; PROTEASE)

Drug : CREON

Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

Application Number : 20725

Country : US

Patented : No

Portfolio PDF

Product Web Link

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Corporate PDF

02

ABBVIE

U.S.A

KY/TN Water Professionals

Not Confirmed

DIVALPROEX SODIUM

Drug : DEPAKOTE

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Application Number : 19680

Country : US

Patented : No

Portfolio PDF

Product Web Link

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03

ABBVIE

U.S.A

KY/TN Water Professionals

Not Confirmed

LEVOMILNACIPRAN HYDROCHLORIDE

Drug : FETZIMA

Dosage Form : CAPSULE, EXTENDED RELEASE; ORAL

Application Number : 204168

Country : US

Patented : Yes

Portfolio PDF

Product Web Link

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Digital Content

Website

Corporate PDF

04

DR REDDYS

India

CPhI Korea

Attending

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

ESOMEPRAZOLE MAGNESIUM

Drug : ESOMEPRAZOLE MAGNESIUM

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Application Number : 78279

Country : US

Patented : No

Product Web Link

05

DR REDDYS

India

CPhI Korea

Attending

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

Drug : FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Application Number : 76667

Country : US

Patented : No

Product Web Link

06

DR REDDYS

India

CPhI Korea

Attending

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

ESOMEPRAZOLE MAGNESIUM

Drug : ESOMEPRAZOLE MAGNESIUM

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Application Number : 211571

Country : US

Patented : No

Product Web Link

07

DR REDDYS LABS SA

India

CPhI Korea

Attending

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

BUDESONIDE

Drug : BUDESONIDE

Dosage Form : CAPSULE, DELAYED RELEASE; ORAL

Application Number : 206623

Country : US

Patented : No

Product Web Link

08

DR REDDYS

India

CPhI Korea

Attending

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

ESOMEPRAZOLE MAGNESIUM; NAPROXEN

Drug : NAPROXEN AND ESOMEPRAZOLE MAGNESIUM

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Application Number : 204206

Country : US

Patented : No

Product Web Link

09

BRECKENRIDGE

U.S.A

KY/TN Water Professionals

Not Confirmed

OMEPRAZOLE

Drug : OMEPRAZOLE

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Application Number : 203481

Country : US

Patented : No

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

10

BRECKENRIDGE

U.S.A

KY/TN Water Professionals

Not Confirmed

DULOXETINE HYDROCHLORIDE

Drug : DULOXETINE HYDROCHLORIDE

Dosage Form : CAPSULE, DELAYED REL PELLETS; ORAL

Application Number : 203088

Country : US

Patented : No

Portfolio PDF

Product Web Link

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Only 10 entries up to this point, click to access all

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FDA Listed Dossiers

01

Dosage Form : CAPSULE

TRIETHYL CITRATE

KY/TN Water Professionals

Not Confirmed

Not Confirmed

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EXCIPIENTS BY APPLICATIONS

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Film Formers Plasticizers

01

Nanjing Well Pharmaceutical

China

AGGSpend

Not Confirmed

Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

Dosage Form : Tablet

Grade : Oral

Category : Film Formers & Plasticizers

Brand Name : Triethyl Citrate

Application : Film Formers & Plasticizers

Excipient Details : Triethyl citrate increases the plasticity of pharmaceutical coating materials & is used as a plasticizer in OSDs. It is also used as a surfactant.

Pharmacopoeia Ref : ChP/USP/EP

Technical Specs : NA

Ingredient(s) : Triethyl Citrate

02

Vertellus

U.S.A

AGGSpend

Not Confirmed

Coating Systems Additives

01

Vertellus

U.S.A

AGGSpend

Not Confirmed

Controlled Modified Release

01

Vertellus

U.S.A

AGGSpend

Not Confirmed

Fillers Diluents Binders

01

Nanjing Well Pharmaceutical

China

AGGSpend

Not Confirmed

Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

Dosage Form : Capsule, Tablet

Grade : Oral

Category : Taste Masking

Brand Name : Triethyl Citrate

Application : Taste Masking

Excipient Details : Triethyl citrate increases the plasticity of pharmaceutical coating materials & is used as a plasticizer in OSDs. It is also used as a surfactant.

Pharmacopoeia Ref : ChP/USP/EP

Technical Specs : NA

Ingredient(s) : Triethyl Citrate

Surfactant Foaming Agents

01

Nanjing Well Pharmaceutical

China

AGGSpend

Not Confirmed

Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

Dosage Form : Capsule, Tablet

Grade : Oral

Category : Surfactant & Foaming Agents

Brand Name : Triethyl Citrate

Application : Surfactant & Foaming Agents

Excipient Details : Triethyl citrate increases the plasticity of pharmaceutical coating materials & is used as a plasticizer in OSDs. It is also used as a surfactant.

Pharmacopoeia Ref : ChP/USP/EP

Technical Specs : NA

Ingredient(s) : Triethyl Citrate

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DATA COMPILATION #PharmaFlow

Excipient Market Overview: Roquette, Seqens, Evonik make strategic moves; new guidelines deal with contamination

The pharmaceutical industry has long recognized the critical role excipients or inactive ingredients play in drug formulation and delivery. Excipients can comprise up to 90 percent of a medicine's total ingredients and serve crucial functions as binders, disintegrants, coatings, preservatives, colors, and flavorings. According to recent market research, the pharmaceutical excipients market was valued at US$ 9.27 billion in 2023. It is growing at a compound annual growth rate (CAGR) of 7.03 percent and is projected to reach US$ 18.48 billion by 2032. The main factors driving market growth is an increased demand for multifunctional excipients, coupled with the expanding use of generic medications. The development in the biologics sector and advancements in nanotechnology are also contributing significantly to market growth. Major excipient providers include BASF, Evonik, Merck KGaA owned MilliporeSigma, Gangwal Healthcare, Roquette Frères, DuPont, Croda International, Seqens, Boai NKY Pharmaceuticals, PMC Isochem, Minakem, Kewpie Corporation, Ashland Global, SPI Pharma, Pfanstiehl, Nanjing Well Pharmaceutical, ICE Pharma, Anhui Ribobay Pharmaceutical and Nippon Fine Chemical. View Our Dashboard on Major Excipient Companies in 2024 (Free Excel Available) WHO, India’s CDSCO tighten regulations; new GMP guidelines implemented to curb contamination Last year, the World Health Organization (WHO) issued a health alert linking at least 300 child deaths in the Gambia, Uzbekistan, and Indonesia to the ingestion of contaminated cough syrups containing unacceptable levels of diethylene glycol (DEG) and ethylene glycol (EG). In response to the tragic events, the WHO released two draft appendices to its guideline on good manufacturing practices (GMPs) for excipients this year. Manufacturers are now required to use suitable risk assessment tools to identify and mitigate potential hazards. Since India-made cough syrups had been linked to the deaths, India’s drug regulator — Central Drugs Standard Control Organization (CDSCO) — took steps to prevent contamination, and advised drugmakers to only use pharmaceutical-grade excipients from approved sources. Furthermore, the Indian Health Ministry proposed amendments to the Drugs and Cosmetics Rules, 1945 to include details of excipients on drug labels. While listing all excipients on every strip of medicine may be challenging, the ministry suggested mentioning those causing hypersensitivity on the label. Applicants now mandatorily need to submit evidence of stability and safety of excipients. These regulatory developments have significant implications for excipient manufacturers and pharmaceutical companies worldwide. Leading pharmaceutical excipient firms like Gangwal Healthcare, Sigachi Industries, and Nitika Pharmaceuticals are well-positioned to meet these heightened quality and safety standards, given their long-standing commitment to producing high-quality, compliant excipients. View Our Dashboard on Major Excipient Companies in 2024 (Free Excel Available) Roquette buys IFF’s pharma unit for US$ 2.85 bn; Evonik opens new spray-drying facility in Darmstadt In a significant industry move, France-based Roquette entered into an agreement to acquire IFF's pharma solutions business in a deal valued at US$ 2.85 billion. This acquisition is set to rebalance family-owned Roquette’s portfolio around health and nutrition. The deal is expected to accelerate Roquette’s growth and significantly strengthen its presence in the excipients market. Evonik has opened a new facility for drying aqueous dispersions of its Eudragit polymers at its site in Darmstadt, Germany. The facility will help Evonik meet increasing demand from drugmakers for its oral drug delivery solutions. The plant uses green energy solutions. The company has also partnered University of Mainz to commercialize a new class of polyethylene glycols (PEG) lipids for nucleic acid delivery. Evonik’s Health Care business has been growing its nucleic acid drug and vaccine delivery portfolio. Germany’s Johannes Gutenberg University of Mainz was the first to develop randomized polyethylene glycols (rPEGs). This collaboration aims to expand Evonik’s toolbox of technologies for nucleic acid-based medicines, offering an improved immunogenicity profile for lipid nanoparticle carriers used in mRNA vaccines and therapeutics. Asahi Kasei made significant strides in addressing a pressing industry concern that emerged in 2018 when potentially carcinogenic nitrosamine impurities were detected in several pharmaceuticals. Guided by regional authorities, such as the European Medicines Agency and the US Food and Drug Administration, the pharmaceutical industry has been carrying out extensive assessments and research to identify the cause of these impurities. In response to this challenge, Asahi Kasei developed its Ceolus microcrystalline cellulose with extremely low nitrite levels. The Japanese company achieved nitrite concentrations of 0.1 micrograms per gram or less, which is equivalent to 0.1 parts per million (ppm). The company also started full commercial operation of its second manufacturing facility for Ceolus in Japan, enhancing supply capacity and stability. JRS Pharma and Gujarat Microwax opened a state-of-the-art cotton-based croscarmellose sodium plant in Mehsana, Gujarat (India). This facility aims to produce high-quality excipients that meet global standards, potentially reducing India's dependency on imports and boosting its presence in the global excipient market. The Indian excipient industry accounts for less than 1 percent of the global market share. View Our Dashboard on Major Excipient Companies in 2024 (Free Excel Available) Seqens to advance innovative polymer; biologics, personalized medicine create demand for specialized excipients Recent industry collaborations highlight the ongoing innovation in novel excipients. France’s Seqens, with over 20 years of polymer development experience, was chosen by Pleryon Therapeutics to advance its leading osteoarthritis candidate – an innovative GMP polymer. This collaboration leverages Seqens’ newly expanded and modernized cGMP plant in Aramon, France, demonstrating the industry’s commitment to investing in advanced manufacturing capabilities for novel excipients. The rise of biologics and personalized medicine has created a demand for specialized excipients capable of stabilizing complex molecules and enabling targeted drug delivery. Roquette’s launch of Lycagel Flex, a hydroxypropyl pemix for nutraceutical and pharmaceutical softgel capsules, exemplifies this trend. Built on Roquette’s market-first Lycagel pea starch technology, this plant-based alternative to gelatin offers manufacturers the flexibility to customize formulations for a range of production and end-user needs. The innovative pea starch foundation also underscores the industry’s move towards sustainable bio-based excipients. The trend towards patient-centric drug development has also influenced excipient innovation. Excipients that can improve palatability, ease of swallowing, or enable novel dosage forms (such as orally disintegrating tablets) are in high demand. For example, IFF brought a super disintegrant Ac-Di-Sol, that supports faster disintegration and drug dissolution in oral disintegrating tablets, improving patient experience. View Our Dashboard on Major Excipient Companies in 2024 (Free Excel Available) Our view The heightened regulatory scrutiny on excipients due to product contamination incidents has created a high risk perception and uncertainty around the regulatory acceptance of novel excipients. That said, novel excipients are central to the development of new drug modalities and therapies. Going forward, sustainability will also become an increasingly important factor in excipient selection and development. As the industry innovates towards biologics, personalized therapies, and patient-centric formulations, the role of high-quality, multifunctional excipients will only grow more vital in ensuring drug stability, bioavailability, and patient compliance. Companies that can navigate the complex regulatory landscape, invest in R&D, and offer high-quality, multifunctional excipients will be well-positioned to succeed in this evolving market.

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EXCIPIENTS

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REF. STANDARDS & IMPURITIES

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USP

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Looking for Triethyl Citrate pharmaceutical excipients? Find information on Triethyl Citrate's applications, manufacturers, suppliers, etc. on PharmaCompass.

CHEMISTRY

Browse all information

INACTIVE PHARMA INGREDIENTS

1 Suppliers

1 USDMF

2 Listed Suppliers

FINISHED DOSAGE FORMULATIONS

305 FDF Dossiers Suppliers

22 FDA Listed Dossiers

EXCIPIENTS BY APPLICATIONS

2 Film Formers & Plasticizers

1 Coating Systems & Additives

1 Controlled & Modified Release

1 Fillers, Diluents & Binders

1 Taste Masking

1 Surfactant & Foaming Agents

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow

MARKET PLACE

4 EXCIPIENTS

REF. STANDARDS & IMPURITIES

1 USP

1 Others

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Dosage Form : CAPSULE

Dosage Form : CAPSULE

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Dosage Form : CAPSULE, COATED PELLETS

Dosage Form : CAPSULE, COATED PELLETS

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Dosage Form : CAPSULE, DELAYED ACTION

Dosage Form : CAPSULE, DELAYED ACTION

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Dosage Form : CAPSULE, DELAYED RELEASE

Dosage Form : CAPSULE, DELAYED RELEASE

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Dosage Form : CAPSULE, ENTERIC COATED PELLET...

Dosage Form : CAPSULE, ENTERIC COATED PELLET...

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Dosage Form : CAPSULE, EXTENDED RELEASE

Dosage Form : CAPSULE, EXTENDED RELEASE

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Dosage Form : CAPSULE, HARD GELATIN

Dosage Form : CAPSULE, HARD GELATIN

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Dosage Form : CAPSULE, SUSTAINED ACTION

Dosage Form : CAPSULE, SUSTAINED ACTION

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Dosage Form : CAPSULE, SUSTAINED ACTION, HAR...

Dosage Form : CAPSULE, SUSTAINED ACTION, HAR...

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Dosage Form : GRANULE, FOR ORAL SUSPENSION

Dosage Form : GRANULE, FOR ORAL SUSPENSION

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