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Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with an equal or greater quantity of an isoquinoline alkaloid of opium [3] [note 1] 9804 Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with one or more active, nonnarcotic ingredients in ...
Schedule 8 (S8) drugs and poisons, otherwise known as Controlled Drugs, are schedule 9 prohibited substances that are appropriate preparations for therapeutic use which have high potential for abuse and addiction. The possession of these medications without authority is the same as carrying a prohibited substance and is illegal.
The Schedule 3 list is one of three lists. Chemicals which can be used as weapons, or used in their manufacture, but which have no, or almost no, legitimate applications as well are listed in Schedule 1, whilst Schedule 2 is used for chemicals which have legitimate small-scale applications. The use of Schedule 1, 2, or 3 chemicals as weapons is ...
Schedule 3/Schedule III may refer to: Third Schedule of the Constitution of India, relating to oaths and affirmations; Schedule III Controlled Substances within the US Controlled Substances Act; Schedule III Controlled Drugs and Substances within the Canadian Controlled Drugs and Substances Act
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met.
Guidance for Industry. [23] This guidance provides sponsors and review staff with the Agency’s thinking about the problems posed by multiple endpoints in the analysis and interpretation of study results and how these problems can be managed in clinical trials for human drugs, including drugs subject to licensing as biological products.
This may also include recommendations on vaccination schedules, such as the appropriate timing, dosage, and contraindications of vaccines. [3] To ensure that the government gives proper attention to NITAG recommendations, the committee typically reports to high-level officials within the Ministry of Health.
Some organisations provide guidance on specification-writing for their staff and partners. [8] [9] In addition to identifying the specific attributes required of the goods or services being purchased, specifications in the public sector may also make reference to the organisation's current corporate objectives or priorities. [8]: 3