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The Omnia series is a line of smartphones produced by Samsung Electronics. Omnia devices run either Microsoft's Windows Mobile 6.5, or Windows Phone 7 operating systems, [1] [2] and one Symbian device under the brand was also released. Samsung Omnia M is a last Omnia phone marketed by Samsung before being superseded by Ativ in Autumn 2012.
This is the list of Schedule I controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required for substances to be placed in this schedule: [2]
A new model with improved specifications and design called the i8000 Samsung Omnia II. [6] [7] Samsung Omnia II GT-I8000(H/L/U) is a multimedia smartphone announced at Samsung Unpacked on June 15, 2009. [8] Earlier Omnia II releases runs Windows Mobile 6.1, however it's upgradable to version 6.5. There is also an unofficial and highly ...
This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage. See the list of FDA-approved therapeutic monoclonal antibodies in the monoclonal antibody therapy page.
Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs.In the majority of circumstances, drugs have 3 types of names: chemical names, the most important of which is the IUPAC name; generic or nonproprietary names, the most important of which are international nonproprietary names (INNs); and trade names, which are brand names. [1]
List of Antiviral Drugs Antiviral Use Manufacturer Component Type Year approved Abacavir: HIV: ViiV Healthcare: Nucleoside analogue reverse transcriptase inhibitor (NRTI) 1998 Acyclovir (Aciclovir) Herpes Simplex, chickenpox, [2] varicella zoster virus: GSK: guanosine analogue RTI 1981 Adefovir: Hepatitis B [3] Gilead Sciences RTI 2002 , 2003 ...
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The national drug code (NDC) is a unique product identifier used in the United States for drugs intended for human use. The Drug Listing Act of 1972 [ 1 ] [ 2 ] requires registered drug establishments to provide the Food and Drug Administration (FDA) with a current list of all drugs manufactured, prepared, propagated, compounded, or processed ...
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