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	<title>Translations:Insulin analog/20/en - Revision history</title>
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	<updated>2026-09-08T21:13:45Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wiki.tiffa.net/w/index.php?title=Translations:Insulin_analog/20/en&amp;diff=130156&amp;oldid=prev</id>
		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2024-03-19T08:49:44Z</updated>

		<summary type="html">&lt;p&gt;Importing a new version from external source&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;==Timeline==&lt;br /&gt;
* 1922 Banting and Best use bovine insulin extract on human&lt;br /&gt;
* 1923 [[Eli Lilly and Company]] (Lilly) produces commercial quantities of bovine insulin&lt;br /&gt;
* 1923 Hagedorn founds the Nordisk Insulinlaboratorium in Denmark forerunner of [[Novo Nordisk]]&lt;br /&gt;
* 1926 [[Novo Nordisk|Nordisk]] receives Danish charter to produce insulin as a non-profit&lt;br /&gt;
* 1936 Canadians D.M. Scott and A.M. Fisher formulate zinc insulin mixture and license to Novo&lt;br /&gt;
* 1936 Hagedorn discovers that adding protamine to insulin prolongs the effect of insulin&lt;br /&gt;
* 1946 Nordisk formulates Isophane porcine insulin a.k.a. Neutral Protamine Hagedorn or [[NPH insulin]]&lt;br /&gt;
* 1946 Nordisk crystallizes a protamine and insulin mixture&lt;br /&gt;
* 1950 Nordisk markets NPH insulin&lt;br /&gt;
* 1953 Novo formulates Lente porcine and bovine insulins by adding zinc for longer-lasting insulin&lt;br /&gt;
* 1978 [[Genentech]] develop biosynthesis of recombinant human insulin in &amp;#039;&amp;#039;Escherichia coli&amp;#039;&amp;#039; bacteria using recombinant DNA technology&lt;br /&gt;
* 1981 Novo Nordisk chemically and enzymatically converts porcine insulin to &amp;#039;human&amp;#039; insulin (Actrapid HM)&lt;br /&gt;
* 1982 [[Genentech]] synthetic &amp;#039;human&amp;#039; insulin approved, in partnership with Eli Lilly and Company, who shepherded the product through the U.S. [[Food and Drug Administration]] (FDA) approval process&lt;br /&gt;
* 1983 Lilly produces biosynthetic recombinant &amp;quot;rDNA insulin human INN&amp;quot; (Humulin)&lt;br /&gt;
* 1985 [[Axel Ullrich]] sequences the human insulin receptor&lt;br /&gt;
* 1988 Novo Nordisk produces synthetic, recombinant insulin (&amp;quot;insulin human INN&amp;quot;)&lt;br /&gt;
* 1996 Lilly Humalog &amp;quot;insulin lispro INN&amp;quot; approved by the U.S. Food and Drug Administration&lt;br /&gt;
* 2003 [[Aventis]] Lantus &amp;quot;glargine&amp;quot; insulin analogue approved in USA &lt;br /&gt;
* 2004 [[Sanofi Aventis]] Apidra insulin &amp;quot;glulisine&amp;quot; analogue approved in the USA.&lt;br /&gt;
* 2006 Novo Nordisk&amp;#039;s Levemir &amp;quot;insulin detemir INN&amp;quot; analogue approved in the USA-&lt;br /&gt;
* 2013 Novo Nordisk&amp;#039;s Tresiba &amp;quot;insulin degludec INN&amp;quot; analogue approved in Europe (EMA with additional monitoring]&lt;/div&gt;</summary>
		<author><name>FuzzyBot</name></author>
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