Drug names of late are very flowing and 'associate' themselves with what they're supposed to do. In the old days, they just used the generic term, and they had hideous, scientific names with massive endings to them (-cillins, -zines, and so forth) but now the names 'suggest' what they'll do for you. "Viagra" hmmm--you'll be viable, and gra is kinda like GROW...... Allegra...gee, in romance languages, that's like happy, you'll be happy without a noseful of snot....Restoral...Oi, if only I could get some REST I'd feel RESTORED.....
So, you may want to combine what the drug actually does (ease breathing, improve lung function, or what have you) and come up with a suggestive word (easy, air, airy, breathe, breeze, breezy, expand/expansive, open, fresh, clean....) and maybe find a way to combine that word, or a loose approximation of that word, with Keith's name, initials or favorite activity.
And then, you have to make sure some other bum hasn't copyrighted it ahead of you! This might help in setting your mind to the task--it's from the FDA, so there's no copyright on it (and thus no need for that four paragraph rule):
Satisfying the FDA
Every drug usually has three names: chemical, generic (non-proprietary), and brand (proprietary), and each is subject to different rules and regulations. The chemical name specifies the chemical structure of the drug. It is not preapproved by any organization, nor is it recognized in any standard manuals, such as USP publications. Therefore, chemical names are primarily used by researchers, but not in medical practice.
The FDA requires that either the established, or official, name or in the absence of an official name, the common or usual name, appears on labels and labeling of a drug product. The common name, loosely referred to as the generic name, must accompany the brand name, if there is one. The established name for a drug substance is usually found in the originating country's pharmacopeia, an official book or list of drugs and medicines and the standards established for their production, dispensation, and use.
The generic name is usually created for drug substances when a new drug is ready for marketing. It is selected by the United States Adopted Names (USAN) Council, whose expertise is recognized by the FDA, according to principles developed to ensure safety, consistency, and logic. These names are typically used by health care professionals.
Generic names are coined using an established stem, or group of letters, that represents a specific drug class. For example, the USAN stems include suffixes like -mab for monoclonal antibodies, such as infliximab, or prefixes like dopa- for dopamine receptor agonists. The arthritis medications celecoxib, valdecoxib, and rofecoxib are generic names containing the -coxib stem. Each belongs to a class of drugs known as the COX-2 inhibitors.
Names that include such stems, chemistry roots, or any other coded information are easier to remember, and give clues about what a drug is used for. These names, however, typically sound or look so much alike that they contribute to medication errors, especially if the products share common dosage forms and other similarities.
The brand name, also called trademark, can be created as soon as a generic name has been established. Only brand names of products subject to a new drug application or an abbreviated new drug application must be approved by the FDA first. This requirement distinguishes them from generic names.
According to a report in the January-February 2004 issue of the Journal of the American Pharmacists Association, there are more than 9,000 generic drug names and 33,000 trademarked brand names in use in the United States.
http://www.fda.gov/fdac/features/2005/405_confusion.htmlYou have a great face--and a unique avatar! Let us know when you get that name established!