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  2. NCAA banned substances - Wikipedia

    en.wikipedia.org/wiki/NCAA_banned_substances

    Alcohol, more precisely ethanol, is a colorless flammable liquid that is the intoxicating agent in fermented and distilled liquors. Beta blockers are any of a group of drugs that decrease the rate and force of heart contractions and lower high blood pressure.

  3. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    The United States Drug Enforcement Administration (DEA) maintains lists regarding the classification of illicit drugs (see DEA Schedules).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.

  4. Controlled Substances Act - Wikipedia

    en.wikipedia.org/wiki/Controlled_Substances_Act

    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.

  5. EMA's safety committee recommends label update for certain ...

    www.aol.com/news/emas-safety-committee...

    (Reuters) - The European Medicines Agency's (EMA) safety committee on Friday recommended changes to product information for all medicines that contain the ingredient pseudoephedrine to address ...

  6. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    Pseudoephedrine is excreted through urine, and the concentration in urine of this drug shows a large inter-individual spread; that is, the same dose can give a vast difference in urine concentration for different individuals. [123] Pseudoephedrine is approved to be taken up to 240 mg per day.

  7. Clandestine chemistry - Wikipedia

    en.wikipedia.org/wiki/Clandestine_chemistry

    Changes to federal regulations in 1988 and throughout the 1990s enabled the DEA to more closely track the ephedrine and pseudoephedrine precursors. [8] Many individual States have enacted precursor control laws which limit the sale of over-the-counter cold medications which contain ephedrine or pseudoephedrine. [14]

  8. Ephedrine - Wikipedia

    en.wikipedia.org/wiki/Ephedrine

    The cinnamoyl-CoA is then reacted with a hydratase to attach the alcohol functional group. The product is then reacted with a retro-aldolase, forming benzaldehyde. Benzaldehyde reacts with pyruvic acid to attach a 2-carbon unit. This product then undergoes transamination and methylation to form ephedrine and its stereoisomer, pseudoephedrine. [89]

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