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The following findings are required, by section 202 of that Act, for substances to be placed in this schedule: The drug or other substance has a high potential for abuse. The drug or other substance has a currently accepted medical use in treatment in the United States or a currently accepted medical use with severe restrictions.
The Schedule 2 list is one of three lists. Chemicals that can be used as weapons, or used in their manufacture, but that have no, or almost no, legitimate applications as well are listed in Schedule 1, whilst Schedule 3 is used for chemicals that also have widespread industrial uses. The use of Schedule 1, 2, or 3 chemicals as weapons is banned ...
With a few exceptions, only annually produced quantities above 100 kg of List 2 substances from Part A or 1000 kg of a precursor from Part B must be reported to the OPCW by the Contracting States. A limit of 1 kg applies to the substance BZ in List 2. For substances in List 3, a threshold value of 30 tonnes applies. [3]
It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs. The list is designated within the Controlled Substances Act [ 1 ] but can be modified by the U.S. Attorney General as illegal manufacturing practices change.
Schedule 2 may refer to: Second Schedule of the Constitution of India, about the rights of government officials; Schedule II Controlled Substances within the US ...
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Controlled Substances; Long title: An Act to amend the Public Health Service Act and other laws to provide increased research into, and prevention of, drug abuse and drug dependence; to provide for treatment and rehabilitation of drug abusers and drug dependent persons; and to strengthen existing law enforcement authority in the field of drug abuse.
Proceedings to add, delete, or change the schedule of a drug or other substance may be initiated by the Drug Enforcement Administration (DEA), the Department of Health and Human Services (HHS), or by petition from any interested party, including the manufacturer of a drug, a medical society or association, a pharmacy association, a public ...