Search for: "United States v. Articles of Food and Drug" Results 61 - 80 of 505
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9 Aug 2011, 7:03 pm by FDABlog HPM
  FDC Act § 201(g)(1) defines “drug” to include articles recognized in the official Homeopathic Pharmacopeia of the United States (“HPUS”) or National Formulary (“NF”). [read post]
31 Mar 2023, 9:31 am by Aaron Black
The Act states that no controlled substance that is a prescription drug as determined under the Federal Food, Drug, and Cosmetic Act may be delivered, distributed, or dispensed by means of the Internet without a valid prescription. [read post]
10 Apr 2009, 8:48 am
New York City Board of Health (pdf), the United States Court of Appeals for the Second Circuit upheld a New York City law requiring restaurant chains to post calorie information on their menus. [read post]
14 Nov 2014, 11:55 am by Kevin
Various Items of Drug Paraphernalia; United States v. [read post]
“Specialty drugs” are a fast growing sector of the pharmaceutical industry and are predicated to represent 50 percent of drug expenditures in the United States by 2020.[1] Specialty drugs are typically dispensed by specialty pharmacies. [read post]
22 Feb 2008, 1:30 pm
In a crushing blow to consumers, on Thursday, February 21st, the United States Supreme Court again sided with big pharmaceutical medical device makers. [read post]
9 Sep 2013, 10:03 pm by Daniel B. Cohen
Food and Drug Administration’s Proposed Produce Rule is a substantively defective product. [read post]
19 Sep 2008, 7:13 am
This Constitution, and the Laws of the United States which shall be made in Pursuance thereof; and all Treaties made, or which shall be made, under the authority of the United States, shall be the supreme Law of the land; and the Judges in every State shall be bound thereby, any Thing in the Constitution or Laws of any State to the Contrary notwithstanding. [read post]
10 Feb 2014, 2:01 am by Lawrence B. Ebert
Indeed, Japan has a record of allowing approximately 14% of patents that are granted in the United States. [read post]
3 Mar 2008, 9:12 pm
[is] not liable . . . if (1) the warnings or information that accompanied the product in its distribution were those approved by the United State Food and Drug Administration. [read post]
4 Apr 2012, 1:41 pm by John J. Sullivan
  The FDA’s powers come from the Federal Food, Drug & Cosmetics Act (“FDCA”). [read post]
21 Nov 2012, 5:00 am by Bexis
  The FDCA, in turn, defines “drug” as:(A) articles recognized in the official United States Pharmacopœia, official Homœopathic Pharmacopœia of the United States, or official National Formulary, or any supplement to any of them; and (B) articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals; and (C) articles (other than… [read post]
It was against this backdrop in November 2022 that a coalition of pro-life and Christian medical organizations filed a lawsuit claiming that the Food and Drug Administration (FDA) had failed to protect “America’s women and girls when it chose politics over science and approved chemical abortion drugs for use in the United States. [read post]
12 Feb 2019, 8:35 am by Joy Waltemath
Her claim that Walmart retaliated against her for pursuing her rights under the state’s workers’ compensation law also failed (Whitmire v. [read post]