According to the FDA's letter-grade system for drug safety during pregnancy, most psychotropic drugs pose a potential risk to the fetus.
those who produce psychotropic drugs or change the production plan or produce additional kinds of psychotropic drugs without authorization;
Article 6 Raw materials of psychotropic drugs and psychotropic drugs shall be allotted by the State according to plan. No production unit shall be allowed to sell them without authorization.
The labels of narcotic drugs, psychotropic drugs, poisonous drugs, radioactive drugs and drugs for external use only must bear the prescribed mark.
The drug dealer unit and the medical treatment unit are not allowed to alter the purchasing certificates and the prescriptions for psychotropic drugs.
Without authorization, no production unit shall be allowed to change the production plan of psychotropic drugs.
The annual production plan for raw materials of psychotropic drugs and for the psychotropic drugs of category I shall be made jointly by the Ministry of Public Health and the State Administration for Medicine.
The import record keeping of narcotics and psychotropic drugs refers to the process that the import entities file applications to the drug administrations where the ports are located for Imported Drugs Port Inspection Notice.
Finished products for psychotropic drugs of category II shall only be transferred to manufacturers with the qualification for designated production.
those who import or export psychotropic drugs without authorization.
A psychotropic drug or other agent.
The term can be scary, but use of psychotropic drugs is often effective, if only temporarily.
Article13 the transportation units must strengthen administration work to ensure prompt shipment of psychotropic drugs by shortening its storage time at the station, on the dock or at the airport.
