What are pharmaceutical intermediates? 

Pharmaceutical intermediates refer to some chemical raw materials or chemical products used in the process of pharmaceutical synthesis. The chemical product does not require a pharmaceutical production license and can be produced in a general chemical plant. As long as it reaches a certain level, it can be used for drug synthesis. After more than 30 years of development, the chemical raw materials and intermediates required for my country's pharmaceutical production can basically be matched, and only a small part of it needs to be imported. Due to China's abundant resources, the price of raw materials is low

API (Active Pharmaceutical Ingredient) refers to the active ingredients contained in medicines. For example, analgesics contain active ingredients that relieve pain. This is the API. A small amount of active ingredients is effective, so there are very few active ingredients in the medicine. You will find the name and quantity of the active ingredients contained in the medicine on the packaging of the over-the-counter medicine.

How APIs are made?

Due to the similar usage of the terms "raw material" and "raw material", they are often confused. Differences Between Pharmaceutical Intermediates And API? Raw material refers to the compound used as a raw material to make an API. We source raw materials from Japanese and international raw material or chemical product manufacturers. When using raw materials, as an API manufacturer, we produce APIs in large reactors in our factories. The API is not produced by a reaction of the raw materials, but through several compounds to become the API. Chemical compounds that are becoming APIs

Strengthen your supply of pharmaceutical intermediates--Nudlehealth

Manufacturers of life-saving drugs and active pharmaceutical ingredients (API) require the most solid supply chain, quality assurance, and regulatory expertise.

Who makes APIs?--Nudlehealth

First of all, as an API manufacturer, we have to consider how to make compounds into APIs in the laboratory. We must also consider the degree of concentration and what temperature can effectively produce high-quality APIs. In order to find the answers to these questions, the staff of our development department began a series of experiments. Once they decide how to make this compound, employees in our production department will use our factory’s large reactors to produce large quantities of APIs.

Then our quality control personnel conduct analysis in the testing laboratory to check whether the produced API is ultra-pure. As you can see, before the final API is manufactured, a considerable number of people are involved in the production phase.

We produce APIs, and pharmaceutical manufacturers use APIs to produce drugs. In addition to the bulk drug, the drug also contains a variety of pharmaceutical excipients. Pharmaceutical manufacturers produce medicines by mixing raw materials and pharmaceutical excipients. This is how the API becomes a drug. It was taken to hospitals and pharmacies until it reached the patient. If an API is not ultra-pure, then it cannot meet strict quality standards, so the quality of the API is very important.