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Your search for “ ���� Cattle Ivermectin ���� www.Ivermectin-Stromectol.com ���� Guinea Pig Mites Ivermectin ���� Oral Ivermectin , Ivermectin Pi” returned the following results.
…tobacco packages, including “color graphics depicting the negative health consequences of smoking,” (2) the restrictions on distribution of samples, continuity programs, and promotion of brands through event sponsorship and merchandise,…
…for line extensions of oral solid dosage form innovator drugs, not only to new formulations, but new indications, combination products, and products marketed by companies independent of the company marketing…
…was represented by Hyman, Phelps & McNamara P.C.) (reply briefs here, here, and here), Judge Huvelle upheld FDA’s decision not to grant a period of 3-year Hatch-Waxman exclusivity in connection…
…patent”) covering ANGIOMAX (bivalirudin). As most folks know by now, FDA approved ANGIOMAX at 5:18 PM on Friday, December 15, 2000 under NDA No. 020873, and MDCO submitted its PTE…
…District Court for the Northern District of Georgia (Atlanta Division) based on federal diversity jurisdiction, the Plaintiffs alleged, among other things, that the decedent, George L. Frazier, ingested Mylan’s 100…
…issued on May 18, 2010, is listed with a “U-642” PUC, defined as “TREATMENT AND PREVENTION OF OSTEOPOROSIS,” and the ‘957 patent, which issued on August 12, 2008, is listed…
…source drug products without an NDA, the [RLD] generally will be the market leader as determined by FDA on the basis of commercial data.” FDA, Final Rule, ANDA Regulations, 57…
…of Health and Human Services (“HHS”) decision to exclude their participation in federal healthcare programs. In May 2007, Purdue pleaded guilty to a felony violation of the Federal Food, Drug,…
…the recent Lauren Stevens case, however, that if a company pays a physician to provide an educational presentation to doctors, the manufacturer is subject to criminal prosecution if that physician…
…oral communication. It documents what information was provided, when, and to whom. Registrants should provide as much information about the incident as possible, including controlled substance quantity and the circumstances…
…client to perpetrate a crime or fraud.” Second, the Court stated that Ms. Stevens’ former employer, GSK, “did not come to Ms. Stevens and say, assist us in committing a…
…ABA v. FTC, No. 1:09-cv-01636, Mar. 4, 2010. The ruling stemmed from Congress’ enactment of the Red Flag Program Clarification Act of 2010 (“Clarification Act”) on December 18, 2010, Public…
…– Amlodipine, Hydrochlorothiazide, and Valsartan Tablets, 5 mg/12.5 mg/160 mg, 5 mg/25 mg/160 mg, 10 mg/25 mg/160 mg, and 10 mg/25 mg/320 mg (EXFORGE HCT) In a second instance…
…of what the FTC will conclude is a serious message conveyed in an advertisement. Furthermore, the FTC ruled that disclaimers and qualifiers such as “preliminary,” “promising,” “encouraging,” “hopeful,” “initial,” and…
…emtricitabine, tenofovir disoproxil fumarate) Tablets (Docket No. FDA-2013-P-0058), PREPOPIK (sodium picosulfate, magnesium oxide and citric acid) for Oral Solution (Docket No. FDA-2013-P-0119), and NATAZIA (estradiol valerate and estradiol valerate/dienogest) Tablets…