D398 Final
2025/2026
Exam Prep Guide
(Expert Verified Questions and
Answers)
Plus A+ Grade Guarantee
, D398 D398
Study online at https://quizlet.com/_dlgzwp
1. What are drug stan- rules that drug manufactures must follow when they produce drugs
dards?
2. 1906 Pure Food and est. drug standards for strength, purity, and quality. also mandated that drugs
Drug Act with with dangerous ingredients be labeled as such
3. 1938 Federal Food, established the Food and Drug Administration (FDA), which is meant to
Drug, and Cosmetic enforce rules such as labeling, drug approval before release, and warning
Act labels
4. 1970 Controlled Act established the Drug Enforcement Agency (DEA). This act set strict stan-
Substances Act dards for abused drugs and required prescribers to register with the DEA.
The DEA enforces the laws included in this act.
5. medication guides paper handouts that come with many prescription medicines. The guides
address issues specific to particular drugs and drug classes, and they con-
tain FDA-approved information that can help patients avoid serious adverse
events.
6. controlled sub- drug that is further categorized into 5 schedules based on the risk of depen-
stances dence and abuse
7. what is the purpose protect the public form potentially dangerous drugs and to regulate how
of drug schedules these drugs can be manufactures and distributed by healthcare facilities
8. schedule I drugs heroin, have the highest risk of abuse and are not approved for medical use
in the US
9. Schedule II drugs psychostimulants (amphetamine) and opioid=based medications (mor-
phine) that have a high risk of abuse and dependence but have accepted
medical uses
10. schedule III drugs certain barbiturate sedatives and anabolic steroids with moderated to low
abuse and dependence risk
2025/2026
2025/2026
Exam Prep Guide
(Expert Verified Questions and
Answers)
Plus A+ Grade Guarantee
, D398 D398
Study online at https://quizlet.com/_dlgzwp
1. What are drug stan- rules that drug manufactures must follow when they produce drugs
dards?
2. 1906 Pure Food and est. drug standards for strength, purity, and quality. also mandated that drugs
Drug Act with with dangerous ingredients be labeled as such
3. 1938 Federal Food, established the Food and Drug Administration (FDA), which is meant to
Drug, and Cosmetic enforce rules such as labeling, drug approval before release, and warning
Act labels
4. 1970 Controlled Act established the Drug Enforcement Agency (DEA). This act set strict stan-
Substances Act dards for abused drugs and required prescribers to register with the DEA.
The DEA enforces the laws included in this act.
5. medication guides paper handouts that come with many prescription medicines. The guides
address issues specific to particular drugs and drug classes, and they con-
tain FDA-approved information that can help patients avoid serious adverse
events.
6. controlled sub- drug that is further categorized into 5 schedules based on the risk of depen-
stances dence and abuse
7. what is the purpose protect the public form potentially dangerous drugs and to regulate how
of drug schedules these drugs can be manufactures and distributed by healthcare facilities
8. schedule I drugs heroin, have the highest risk of abuse and are not approved for medical use
in the US
9. Schedule II drugs psychostimulants (amphetamine) and opioid=based medications (mor-
phine) that have a high risk of abuse and dependence but have accepted
medical uses
10. schedule III drugs certain barbiturate sedatives and anabolic steroids with moderated to low
abuse and dependence risk
2025/2026
