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Ketotifen Impurities: Focusing on Quality Control of a Classic Antihistamine Drug

Ketotifen Impurities: Focusing on Quality Control of a Classic Antihistam...

Ketotifen, as a first-generation antihistamine, exerts its effects by strongly blocking H1 histamine receptors, thereby counteracting allergic symptoms such as bronchial smooth muscle contraction an...

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Overcoming quality inspection challenges: Complete set of famotidine impurities available

Overcoming quality inspection challenges: Complete set of famotidine impuritie...

Famotidine is a third-generation, highly effective H2 receptor antagonist primarily used to inhibit gastric acid secretion, treating conditions such as gastric and duodenal ulcers, and gastroesophag...

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Full Range Available Now! Supporting Paclitaxel Impurity Research

Full Range Available Now! Supporting Paclitaxel Impurity Research...

Paclitaxel is a diterpenoid compound isolated and purified from plants of the Taxaceae family. It is a classic anticancer drug widely used globally, known for its ideal efficacy and low toxicity....

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Atorvastatin Impurities: A Key Role in Hyperlipidemia Control and Prevention

Atorvastatin Impurities: A Key Role in Hyperlipidemia Control and Preven...

With the expansion of the atorvastatin market and the emergence of generic versions, drug quality and impurity control have become critical links in ensuring the efficacy and safety of this important...

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FDA Approves Wegovy® Pill, Ushering in a New Era of Oral Obesity Treatment

FDA Approves Wegovy® Pill, Ushering in a New Era of Oral Obesity Tr...

Novo Nordisk announced that the U.S. Food and Drug Administration (FDA) has approved Wegovy® tablets (containing 25 mg of semaglutide for once-daily oral administration) to help reduce exc...

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world first!A New Treatment Option for DPNP and the Critical Control of Key Drug Impurities

world first!A New Treatment Option for DPNP and the Critical Control ...

Recently, the Lidocaine Gel Patch (brand name: DeBaiNing®), developed by Tide Pharm, a subsidiary of China Biopharmaceuticals, has been granted approval for a new indication by the Nation...

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A Key Strategy for Mastering Pimecrolimus Impurity Quality Control

A Key Strategy for Mastering Pimecrolimus Impurity Quality Control...

Pimecrolimus cream is a non-hormonal topical dermatological formulation. The 1% pimecrolimus cream is approved for the treatment of mild to moderate atopic dermatitis (AD) in non-immunocompromised...

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Diverse Options in Influenza Prevention and Control: How to Ensure Drug Quality

Diverse Options in Influenza Prevention and Control: How to Ensure Drug ...

As the flu season persists, drug quality control becomes a critical link in ensuring public medication safety. Drug impurity reference standards, serving as the "benchmark" in drug quality research,...

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Atrasentan Impurities—A Critical Quality Control Factor in IgA Nephropathy Treatment

Atrasentan Impurities—A Critical Quality Control Factor in IgA Nephro...

In August 2025, atrasentan hydrochloride tablets were officially approved by China‘s National Medical Products Administration (NMPA) for the reduction of proteinuria in adult patients wi...

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Full Set In Stock | Adrenaline Impurities Now Shining Bright!

Full Set In Stock | Adrenaline Impurities Now Shining Bright!...

SZEB specializes in supplying Adrenaline impurity reference standards, including the N-NitrosoAdrenaline series and Adrenaline EP impurity series, to meet diverse experimental needs. Thes...

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Combination Nasal Spray Ryaltris® Disrupts the Rhinitis Market: How Were the Impurity Challenges of Olopatadine and Mometasone Overcome?

Combination Nasal Spray Ryaltris® Disrupts the Rhinitis Market: How We...

On November 10th, the compound nasal spray containing Olopatadine Hydrochloride and Mometasone Furoate (brand name: Ryaltris®), jointly developed by Grand Pharmaceutical Group‘s subsidiary...

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Xanomeline : A Pioneering Non-Dopaminergic Therapy

Xanomeline : A Pioneering Non-Dopaminergic Therapy...

The fixed-dose combination drug Cobenfy (Kar XT), composed of xanomeline and trospium chloride, received FDA approval in September 2024 for the treatment of schizophrenia in adults. This mar...

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In Stock | Sacubitril impurity references

In Stock | Sacubitril impurity references...

Sacubitril Valsartan Sodium Tablets is the world‘s first commercially available angiotensin receptor-neprilysin inhibitor (ARNI). It was approved for marketing in 2017 by the National Medi...

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Udenafil Impurity Control and Scientific Innovation: Professional Pharmaceutical Enterprise Reference Standard Solutions

Udenafil Impurity Control and Scientific Innovation: Professional Pharmac...

Udenafil is a selective phosphodiesterase type 5 (PDE5) inhibitor. It is primarily used for the treatment of male erectile dysfunction (ED) and is also applied in the management of premature ej...

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China’s First Domestically Developed Dulaglutide Injection Approved for Market Launch, Ushering in a New Landscape for GLP-1 Drugs​

China’s First Domestically Developed Dulaglutide Injection Approved for ...

On August 8, Boan Biotechnology announced that its independently developed Boyouping® (Dulaglutide Injection) has received market approval from the National Medical Products Administration...

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Crisaborole is Reshaping Atopic Dermatitis Treatment, Backed by SZEB Quality Control Support​

Crisaborole is Reshaping Atopic Dermatitis Treatment, Backed by SZEB Q...

Crisaborole is a boron-containing small-molecule anti-inflammatory drug, classified as a non-steroidal topical phosphodiesterase-4 (PDE-4) inhibitor. By inhibiting PDE-4, the drug increases th...

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Qilu Pharmaceutical Co.,Ltd.’s Carfilzomib for Injection Approved for Market Launch

Qilu Pharmaceutical Co.,Ltd.’s Carfilzomib for Injection Approved for M...

Qilu Pharmaceutical Co.,Ltd’s Carfilzomib for Injection has received market approval from the National Medical Products Administration (NMPA) of China for the treatment of adult patie...

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First-in-Class: FDA OKs Triple Therapy to Treat Hypertension

First-in-Class: FDA OKs Triple Therapy to Treat Hypertension...

Recently, George Medicines announced that its new drug Widaplik® (containing telmisartan, amlodipine, and indapamide, previously known as GMRx2) has been approved by the U.S. Food and Drug...

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LEQEMBI IQLIK™, the first-ever at-home subcutaneous injection for Alzheimer‘s disease, has been approved.

LEQEMBI IQLIK™, the first-ever at-home subcutaneous injection for A...

The U.S. FDA has approved the lecanemab-irmb subcutaneous injection (U.S. brand name: LEQEMBI IQLIK™), jointly developed by Biogen and Eisai, for maintenance therapy in early A...

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Folic Acid Impurities: Reference Standards for Pharmaceutical Quality Control​

Folic Acid Impurities: Reference Standards for Pharmaceutical Quality Co...

Beyond process-related impurities, factors such as light exposure, high temperatures, or humid conditions can cause the oxidation or degradation of folic acid, leading to the formation of new impurit...

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