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Layanan Pengaduan Konsumen

(Matériel de performance de l’unité commerciale, équipe de soutien aux ventes)

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Gedung AIA Central, Niveau 39, Jl. Jend. Sudirman Kav. 48A, Jakarta Selatan, Indonésie

+62 21 2988 8557

[email protected]

Direktorat Jenderal Perlindungan Konsumen dan Tertib Niaga Kementerian Perdagangan Republik Indonesia
0853 1111 1010

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Ingrédients Pharmaceutiques Actifs (API)

Ingrédients Pharmaceutiques Actifs (API)

Explorez la gamme d’API de haute qualité proposée par DKSH, issue de fournisseurs mondiaux de premier plan. Nous aidons les entreprises pharmaceutiques à garantir conformité réglementaire, sécurité et performance constante des formulations.

Ingrédients Pharmaceutiques Actifs (API)

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BILASTINE

Bilastine is a white to off-white crystalline powder that is sparingly soluble in methylene chloride and practically insoluble in acetone. It has an assay range of 98.0% to 102.0%.

 

Products still subject to third-party patent protection might be available solely for R&D purposes.

DEXTROSE MONOHYDRATE

덱스트로오스 모노하이드레이트는 유기 화합물입니다. 무색 크리스탈 또는 백색 크리스탈 분말, 무취 및 달콤한. 물에 용해되고 에탄올에 약간 용해됩니다.
CALCIUM ASCORBATE

아스코르브산 칼슘은 흰색에서 약간 황색을 띠며 무취의 결정 또는 결정 분말입니다.
DEXMEDETOMIDINE HCL

Dexmedetomidine Hydrochloride (HCl) stands as a pivotal chemical for the pharmaceutical sector, utilized primarily as a sedative, anxiolytic, and analgesic agent. Under the umbrella of performance materials, this product maintains a strong presence within medical settings, with a focus on providing sedation for non-intubated patients before and/or during surgical and other procedures. It's also used in intensive care sedation for intubated, mechanically ventilated patients. Manufactured in adherence to stringent standards, Dexmedetomidine HCl is a white or almost white powder that dissolves freely in DMSO and is slightly soluble in methanol and water, ensuring its ease of adoption in various pharmaceutical formulations. Our product complies with the United States Drug Master File (US DMF), and proudly carries the European Union Good Manufacturing Practice (EU GMP) certification, attesting to its high-grade quality and the thoroughness of its production process. Beyond its uses, this product is defined by its anatomical therapeutic chemical classification, which refers to a system used for the classification of drugs. A prime focus is on organic purity, with individual impurities like Dimethylphenylethyl imidazole and Levomedetomidine meticulously controlled to exceed pharmacopeial standards. Our product boasts a laudable enantiomeric purity and an assay value ranging between 98.0% and 102.0%, exemplifying its consistency and reliability. It is vital to note that our Dexmedetomidine HCl maintains permissible thresholds for residual solvents, ensuring the safety and efficacy of the drug. The list of related substances and required specifications for solvents like acetone, ethanol, and benzene are rigorously quantified below recognized safety limits, aligning with the highest regulatory expectations. We ensure that each batch is synonymous with excellence, a testament to our unwavering commitment to the highest quality standards in pharmaceutical ingredients. By choosing our Dexmedetomidine HCl, stakeholders in the pharmaceutical industry can confidently incorporate a product that is not only potent and versatile but also conforms to the critical parameters of drug safety and manufacturing excellence. For more information, please visit our website or contact our customer service team, who stand ready to assist with product inquiries and logistic details.

 

Products still subject to third-party patent protection might be available solely for R&D purposes.

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