Law 1
Law 2
Law 3
Law 4
Law 5
References
200

This law was enacted in response to unsanitary conditions in the meat packing industry in 1906 and was the first law that required that drugs be proven pure before they could be marketed

what is the Food and Drug Act (1906)

200

Both foreign and domestic drugs require approval by this agency before they can be marketed in the United States

What is the FDA?
200

How long in years all records for controlled substances must be maintained and readily available for inspection by the DEA or Board of Pharmacy

What is 2 years?

200

The class of drug recall issued when there is a strong likelihood of serious adverse reactions or death due to a medication.

What is a Class-I recall

200

This law allowed a patient to request that all of their prescriptions be  placed in containers without safety closures

What is the PPPA of 1970 (Poison Prevention Packaging Act?

200
This reference is officially known as "The FDA's Approved Drug Products with Therapeutic Equivalence Evaluations"

What is the Orange Book

200
This law will be followed when there is a difference between state and federal law.

what is the more strict or stringent law

200

This law allows a pharmacist to dispense sublingual nitroglycerin and metered dose inhalers without safety closures

What is the poison prevention packaging act of 1970?

200

This agency is responsible for issuing licenses to pharmacies, pharmacists and technicians, and for establishing requirements for reference materials in the pharmacy.

what is the BOP (Board of Pharmacy)

200

This paperwork must be provided to a patient the first time they fill a prescription in your pharmacy.

What is the HIPAA Privacy Policy
200

Due to OBRA '90, a pharmacy must offer ______________ to all Medicare and Medicaid patients picking up new prescriptions.

What is counseling?

200

This reference is used to look up Average Wholesale Pricing Information.

What is the Red Book?

200

The class of drug recall issued when there is little chance of a serious adverse event from a drug product

What is a Class III (3) drug recall?

200

This law made is legal for a physician to telephone a new prescription into a pharmacy

What is Durham Humphrey Amendment

200

This law required that health care providers protect the privacy and security of a patient's PHI

What is HIPAA?

200

This amendment to the Food, Drug and Cosmetic Act divided drugs into those that require a prescription and those that are Over-The-Counter.

What is the Durham Humphrey Amendment

200

These two items located on a manufacturer bottle of a medication are used to identify recalled drugs.

What are the NDC number and lot number

200

This reference is where one would check to see if taking two drugs together is safe or not.

What is Drug Interaction Facts

200

OSHA mandates that employees with potential exposure to blood borne pathogens be offered a vaccination for this disease at no charge.

What is Hepatitis B?
200
Due to OBRA '90, all Medicare and Medicaid patients must have this in a pharmacy?

What is a patient profile?

200

In response to the sulfanilamide tragedy that killed over 100 children in the 1930s, this law required that all drugs marketed in the United States be proven safe 

What is the 1938 Food, Drug and Cosmetic Act?

200

The four phases of studies that must occur with human subjects in order to obtain final FDA approval of a drug are called this.

What are clinical trials?

200

Due to OBRA '90, this professional service that screens a patient's profile for contraindications, must be performed by a pharmacist before they fill a prescription for a Medicare or Medicaid patient.

What is prospective DUR

200

The organization that establishes the requirements for reference materials in a particular state.

What is the BOP or Board of Pharmacy

200

This was the first law that required drugs be proven pure, safe and effective before they were sold in the United States.

what is Kefauver Harris/the Kefauver Harris Amendment

200

This law requires that manufacturers provide SDSs (Safety Data Sheets) to accompany all hazardous substances that they sell

What is OSHA of 1970 (Occupational Safety and Health Act)?

200

Pharmacists and prescribers are required to access this system before prescribing or filling prescriptions for controlled substances in order to detect drug diversion.

What are PDMPs (Prescription Drug Monitoring Progams)? CRISP in Maryland

200

This is the length of time the signed HIPAA privacy policy acknowledgement must be retained by a pharmacy.

What is 6 years.

200

These are the two groups of people who are legally able to request that a prescription be dispensed with an easy open cap

Who are the prescriber and the patient?

200

This book is a compilation of manufacturer package inserts

What is the PDR? 

Physicians' Desk Reference

200

This organization is responsible for ensuring that unwanted pharmaceutical and other chemicals do not contaminate the environment or our drinking water

What is the EPA (Environmental Protection Agency)

200

This is the organization that oversees Medicare and Medicaid.

What is CMS

(Center for Medicare and Medicaid Services)

200
This is the number of refills allowed on a C-III or C-IV controlled substance.

What is 5 refills

200

This is the number of refills allowed on a C-II controlled substance.

What is zero

200

This is the number of refills allowed on a C-V controlled substance.

What is as many as the prescriber wrote

200

This is the best reference for stability, storage, purity and identification of a drug, and is the official compendium of pharmaceutical products in the United States.

What is the USP-NF

United States Pharmacopeia- National Formulary

200

This is the form used to order schedule C-II controlled substances.

What is DEA Form 222?

200

This is the minimum age allowed to purchase an exempt narcotic.

What is 18 years old.

200

This is the form used to report the loss or theft of a significant amount of controlled substances.

What is DEA Form 106?

200

When a pharmacy first registers with the local DEA office, they use this form.

What is a DEA 224?

200

DEA Form 41 is used to do this.

What is request permission to destroy unwanted C-II controlled substances?

200
When looking up a generic drug in the Orange Book, only drugs with a bioequivalence rating beginning with this letter are considered substitutable with the brand name product.

What is an "A"?

200

This is the maximum amount of pseudoephedrine that may be purchased in a day.

What is 3.6 grams?

200

Drugs are divided into this many schedules by the Controlled Substance Act, based on their potential for abuse.

What is 5?
200

These kits must be available wherever antineoplastic medications are compounded, stored, delivered or administered

What are Chemo Spill Kits?

200

The middle four numbers in an NDC number indicate this.

What is the drug product?

200

This is the maximum amount of pseudoephedrine that may be purchased in a retail pharmacy without a prescription in a month.

What is 9 grams?

200

A drug rating in the Orange book that begins with this letter is not substitutable for the brand name product.

What is a "B"