BIOEQUIVALENCE;
BIOTECHNOLOGY;
CELL LINE;
COST CONTROL;
DRUG APPROVAL;
DRUG COST;
DRUG FORMULATION;
DRUG INDUSTRY;
DRUG MARKETING;
DRUG METABOLISM;
DRUG SAFETY;
DRUG STRUCTURE;
DRUG SUBSTITUTION;
DRUG SYNTHESIS;
FOOD AND DRUG ADMINISTRATION;
GLYCOSYLATION;
HUMAN;
KIDNEY DISEASE;
LAW SUIT;
NONHUMAN;
PATENT;
PHARMACEUTICAL ENGINEERING;
PHARMACIST;
PRESCRIPTION;
PURE RED CELL ANEMIA;
REVIEW;
UNSPECIFIED SIDE EFFECT;
Potential savings from substituting generic drugs for brand-name drugs: Medical expenditure panel survey, 1997-2000
Haas JS, Phillips KA, Gerstenberger EP, Seger AC. Potential savings from substituting generic drugs for brand-name drugs: medical expenditure panel survey, 1997-2000. Ann Intern Med 2005;142:891-7.
U.S. Food and Drug Administration. Savings from generic drugs purchased at retail pharmacies. Available at http://www.fda.gov/cder/consumerinfo/ savingsfromgenericdrugs.htm. Accessed December 1, 2005.
Biogenerics hang at the starting gate. Generic biopharmaceutical makers seek short-cut approvals from FDA
March
Faden M. Biogenerics hang at the starting gate. Generic biopharmaceutical makers seek short-cut approvals from FDA. Pharmaceutical Business Strategies March 2005. Available at http://www.pbsmag.com/Article.cfm?ID=169. Accessed December 5, 2005.
FDA rebuffs Novartis over delay to biogeneric drug
Hirschler B. FDA rebuffs Novartis over delay to biogeneric drug. Reuters Regulatory News Available at http://yahoo.reuters/com/financeNewsArticle.jhtml? type=government. Accessed December 1, 2005.
U.S. Food and Drug Administration Center for Drug Evaluation and Research. FDA statement on generic Premarin. May 5, 1997. Available at http://www.fda.gov/cder/news/cepressrelease.htm. Accessed November 28, 2005.