Drug labelling is also referred to as prescription labelling, is a written, printed or graphic matter upon any drugs or any of its container, or accompanying...

section of labeling is to enable health care practitioners to readily identify appropriate therapies for patients by clearly communicating the drug's approved...

Pharmacogenomics, often abbreviated "PGx," is the study of the role of the genome in drug response. Its name (pharmaco- + genomics) reflects its combining of pharmacology...

drugs and over-the-counter drugs (OTCs) can be used in off-label ways, although most studies of off-label use focus on prescription drugs. Off-label use...

plainly. In the United States, labelling for the healthcare practitioner is called "Prescribing Information" (PI), and labelling for patients and/or caregivers...

A drug is any chemical substance other than a nutrient or an essential dietary ingredient, which, when administered to a living organism, produces a biological...

food labelling move". 3 News NZ. April 8, 2013. Archived from the original on October 29, 2013. Retrieved April 8, 2013. "Policy Paper: Labelling of sugars...

Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical...

Regulation (EC) No. 834/2007 of 28 June 2007 on organic production and labelling of organic products Regulation (EU) No 1169/2011 Regulation 1151/2012...

The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible...