Behind the prosperity of China's API industry, there are many challenges, which make its development encounter difficulties.Objectively speaking, China is currently the world leader in API, and the market is still expanding.

APIs are generally manufactured through cthat include: Biological and Chemical Processes. How is active pharmaceutical ingredient manufactured? The following is the active pharmaceutical ingredient manufacturing process.

Pharmaceutical raw materials are the substances that are used to manufacture wide range of drug formulations, tablets, capsules, injectable etc. The raw material used in the pharmaceutical industry are consisted of three major parts, they are:² API² Excipients² Packaging.

Elagolix (ABT-620) is an oral gonadotropin-releasing hormone antagonist being studied for the treatment of endometriosis, uterine fibroids and PCOS. For the management of moderate to severe pain associated with endometriosis.

Pregabalin, one of the best-selling prescription drugs in the world, is researched and developed by Pfizer, it has been approved by EMA on 6th July 2004, and approved by FDA on 30th Dec 2004. Trade name is LYRICA.

In the pharmaceutical industry, you might hear the terms “FDF” and “API” frequently used in reference to products. We surely understand this type of jargon, but we certainly can see how the general public would feel overwhelmed looking at those kinds of terminology abbreviations.

Apixaban is used help prevent strokes or blood clots in people who have atrial fibrillation (a condition in which the heart beats irregularly, increasing the chance of clots forming in the body and possibly causing strokes) that is not caused by heart valve disease.

Icotinib (cas no. 610798-31-7) is a epidermal growth factor receptor tyrosine kinase (EGRF-TKI) inhibitor. It is used for treatment of advanced non-small cell lung cancer (NSCLC).

Gilteritinib Fumarate, developed by Astellas, was approved by the Japanese Pharmaceutical Medical Devices And Devices Integrated Agency (PMDA) on 21 September 2018, subsequently approved by the US Food and Drug Administration (FDA) on 28 November 2018, and by the European Drug Administration (EMA) on 24 October 2019 under the trade name Xospata®.

Ursodeoxycholic acid is a cholelithiant commonly used in the gastroenterology department, and also a cholelithiasis dissolving agent, so it can be used in the treatment of gallstones under normal circumstances, on the premise that the gallbladder has normal contraction function.

Misoprostol is a prostaglandin E1 analogue that causes cervical softening and dilation and uterine contractions. Routes of administration include oral, vaginal, rectal, buccal, and sublingual. Misoprostol, a derivative of prostaglandin E1, can be used in the treatment of duodenal ulcer.

Pharmaceutical intermediates are fine chemical products in the production process from pharmaceutical chemical raw materials to bulk drugs or drugs. The synthesis of chemical drugs depends on high-quality pharmaceutical intermediates. This chemical, which does not require a drug production license, can be produced in ordinary chemical plants and can be used in the synthesis of drugs as long as it reaches certain grades.

Intermediates and additives are common in our daily life, for example, vitamins, disperse dyes, bleaches and emulsifiers are collectively called Intermediates and additives. Today, this article focuses on introducing what intermediates are and what are the differences between them and API.

Pharmaceutical intermediates refer to the chemical raw materials or chemical products used in the pharmaceutical synthesis process. From the perspective of the development history of China's pharmaceutical intermediates industry, after nearly 30 years of development, pharmaceutical intermediates have developed from a small branch of the chemical industry into an emerging industry with an output value of billions of yuan, and the market competition has become increasingly fierce.

About Favipiravir Chemical name:Favipiravir; 6-fluoro-3-hydroxypyrazine-2-carboxamide.Molecular formula: C24H29N5O3structural formula：

What is an active pharmaceutical ingredient (API in pharma)? In the pharmaceutical industry, a widely used term is ‘API’, which means Active Pharmaceutical Ingredient and refers to the ingredients or active pharmaceutical substances that can eventually be converted into a medicine.

A review of six Phase 3 studies shows that tofacitinib is more effective for rheumatoid arthritis (RA) treatment than regimens including placebo and a disease modifying anti-rheumatic drug or methotrexate (MTX) as monotherapy or in combination therapy. The efficacy of tofacitinib was similar in pati

Baloxavir marboxilGeneric Name: baloxavir marboxil (ba LOX a vir mar BOX il)Brand Name: XofluzaWhat is baloxavir marboxil?Baloxavir marboxil is used to treat flu symptoms caused by influenza virus in people who have had symptoms for no more than 48 hours. Baloxavir marboxil will not treat the common

On November 2, 2018, the Food and Drug Administration granted accelerated approval to lorlatinib (LORBRENA, Pfizer, Inc.) for patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) whose disease has progressed on crizotinib and at least one other ALK in

RelugolixRelugolix (also known as Relumina, TAK-385, or RVT-601) is a gonadotropin-releasing hormone (GnRH) receptor antagonist being developed and tested by Myovant Sciences. This oral once-daily medicine is intended to treat endometriosis, as well as uterine fibroids and hormone-sensitive prostate