The US Food and Drug Administration (FDA) has approved the "morning-after" pill without a prescription for women aged 15 and over.

BBC: US morning-after pill approved for 15-year-olds

The Food and Drug Administration (FDA) is evaluating the safety of over-the-counter cold and cough medications in older children.

CNN: Cold remedies: What works, what doesn't, what can't hurt

The first approach, known as the Kennedy-Waxman bill, will give the beleaguered Food and Drug Administration (FDA) authority to regulate tobacco.

FORBES: Magazine Article

The stock bolted higher in mid-March, after the findings of a Food and Drug Administration (FDA) review panel led many analysts to conclude that a menthol ban was relatively unlikely.

FORBES: Options Plays On 3 Cig Stocks Smoking The Market

The three drugs are not approved by the Food and Drug Administration (FDA) for treatment of ADHD or long-term treatment of bipolar disorder, nor are they approved for children as young as Rebecca.

FORBES: Bad Side-Effects Ahead For Pharma?

In October, the U.S. Food and Drug Administration (FDA) nixed not one but two new weight-loss drugs, lorcaserin and Qnexa, because of possible links to cancer (lorcaserin) and heart problems (Qnexa).

CNN: Combo of old drugs offers new hope in obesity fight

Bristol-Myers Squibb Company today announced that the U.S. Food and Drug Administration (FDA) has determined that additional time is required to complete the review of the biologics license application (BLA) for ipilimumab in pre-treated advanced melanoma, and has moved its decision date from December 25, 2010 to March 26, 2011.

FORBES: Immune-Boosting Cancer Drug Hits FDA Delay

Both companies, however, will have to deal with a new entrant, Humira, which is made by Abbott Laboratories (nyse: ABT - news - people ) and was just approved by the U.S. Food and Drug Administration (FDA).

FORBES: Magazine Article