Regulatory Affairs Syndicator

WASHINGTON (Reuters) - The first generic version of GlaxoSmithKline’s GSK.L GSK.N widely-used allergy spray Flonase won U.S. approval on Wednesday, but the drugmaker said it might take legal action against the U.S. Food and Drug Administration.

WASHINGTON (Reuters) - GlaxoSmithKline GSK.L GSK.N may take legal action against the U.S. Food and Drug Administration over the agency’s approval of a generic version of its blockbuster allergy drug Flonase, a company spokeswoman told Reuters on Wednesday.

WASHINGTON (Reuters) - The first generic version of GlaxoSmithKline’s widely-used allergy spray Flonase won U.S. approval on Wednesday, but the British drugmaker said it might take legal action against the U.S. Food and Drug Administration.

BOSTON (AFX) — Drug stocks joined in the broader market rally Wednesday, but Sanofi-Aventis was down for the second straight day after receiving two setbacks from the Food and Drug Administration.

WASHINGTON (Reuters) - GlaxoSmithKline ( GSK ) may take legal action against the U.S. Food and Drug Administration over the agency’s approval of a generic version of its blockbuster allergy drug Flonase, a company spokeswoman told Reuters on Wednesday.

The first generic version of GlaxoSmithKline’s widely-used allergy spray Flonase won U.S. approval on Wednesday, but the British drugmaker said it might take legal action against the U.S. Food and Drug Administration.

WASHINGTON (Reuters) - The first generic version of GlaxoSmithKline’s widely-used allergy spray Flonase won U.S. approval on Wednesday, but the British drugmaker said it might take legal action against the U.S. Food and Drug Administration.

BRIDGEWATER — Sanofi-Aventis SA’s weight-loss drug Acomplia may be approvable after the company meets certain conditions, the U.S. Food and Drug Administration says.

WASHINGTON (Reuters) - GlaxoSmithKline ( GSK.L ) may take legal action against the U.S. Food and Drug Administration over the agency’s approval of a generic version of its blockbuster allergy drug Flonase, a company spokeswoman told Reuters on Wednesday.

The Food and Drug Administration in the U.S. has recommended a new vaccine for routine use against rotavirus infection.

The U.S. Food and Drug Administration (FDA) is alerting the public to a recall being conducted by Mead Johnson for their GENTLEASE powdered infant formula, lot number: BMJ19, use by 1 Jul 07. This lot was found to contain metal particles, consisting of up to 2.7 millimeter in size.

The Food and Drug Administration (FDA) has approved Fluticasone Propionate Nasal Spray, the first generic version of the brand name drug Flonase

WASHINGTON, Feb. 22 (UPI) — Progenics said Wednesday its HIV treatment PRO 140 has been given fast-track status by the Food and Drug Administration.

The U.S. Food and Drug Administration clarified its definition of “whole grains” last week, several months after recommending that Americans incorporate more whole grains in their diets.

The U.S. Food and Drug Administration clarified its definition of “whole grains” last week, several months after recommending that Americans incorporate more whole grains in their diets.