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  2. List of Schedule IV controlled substances (U.S.) - Wikipedia

    en.wikipedia.org/wiki/List_of_Schedule_IV...

    This is the list of Schedule IV controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required for substances to be placed in this schedule: [2] The drug or other substance has a low potential for abuse relative to the drugs or other substances in schedule III.

  3. Controlled Substances Act - Wikipedia

    en.wikipedia.org/wiki/Controlled_Substances_Act

    Except when dispensed directly to an ultimate user by a practitioner other than a pharmacist, no controlled substance in Schedule II, which is a prescription drug as determined under the Federal Food, Drug, and Cosmetic Act (21 USC 301 et seq.), may be dispensed without the written or electronically transmitted (21 CFR 1306.08) prescription of ...

  4. Standard for the Uniform Scheduling of Medicines and Poisons

    en.wikipedia.org/wiki/Standard_for_the_Uniform...

    Situations that may require an authority include where the drug may only have benefit in limited conditions, the true cost of the drug is high, or when there is a risk of dependence. Some states have subsets of Schedule 4 with additional requirements (see below). Schedule 4 medicines cannot be advertised directly to the public. Examples:

  5. Auxiliary label - Wikipedia

    en.wikipedia.org/wiki/Auxiliary_Label

    An auxiliary label (also called cautionary and advisory label or prescription drug warning label) is a label added on to a dispensed medication package by a pharmacist in addition to the usual prescription label. These labels are intended to provide supplementary information regarding the safe administration, use, and storage of the medication. [1]

  6. Comprehensive Drug Abuse Prevention and Control Act of 1970

    en.wikipedia.org/wiki/Comprehensive_Drug_Abuse...

    The Comprehensive Drug Abuse Prevention and Control Act of 1970, Pub. L. 91–513, 84 Stat. 1236, enacted October 27, 1970, is a United States federal law that, with subsequent modifications, requires the pharmaceutical industry to maintain physical security and strict record keeping for certain types of drugs. [1]

  7. Poison Prevention Packaging Act of 1970 - Wikipedia

    en.wikipedia.org/wiki/Poison_Prevention...

    Household substances in liquid form containing 4% or more by weight of methyl alcohol (methanol), other than those packaged in pressurized spray containers. Sulfuric acid. Household substances containing 10% or more by weight or sulfuric acid, except substances in wet-cell storage batteries. Prescription drugs.

  8. Convention on Psychotropic Substances - Wikipedia

    en.wikipedia.org/wiki/Convention_on_Psychotropic...

    This allows the nation to comply with a less stringent set of restrictions. The U.S. Controlled Substances Act's 21 U.S.C. § 811(d)(4) implies that placing a drug in Schedule IV or V of the Act is sufficient to "carry out the minimum United States obligations under paragraph 7 of article 2 of the Convention". [18]

  9. Drug packaging - Wikipedia

    en.wikipedia.org/wiki/Drug_packaging

    Internet pharmacies mail the prescribed drugs to the customer; boxes or mailing envelopes are used. Child resistant packaging is often required on the unit packs; if requested, a pharmacist is allowed put drugs in a bottle with easy open features. Over-the-counter drugs are sold in drug stores, grocery stores, and diverse retail outlets.