CHAPTER 3 PHARMACY LAW SUMMER 2022

FOR A PHYSICIAN WHAT WILL THEIR DEA # START WITH?

WHAT DEA FORM IS USED FOR LOSS OR THEFT?

C3 AND C4 CONTROLLED SUBSTANCES CAN HAVE HOW MANY REFILLS OR WHAT TIME LIMIT?

A PATENT ON A NEW DRUG IS GOOD FOR HOW LONG?

WHO IS THE ONLY PERSON THAT IS ALLOWED TO COUNSEL PHARMACY PATIENTS?

HOW MANY REFILLS CAN REGULAR LEGEND DRUGS HAVE?

WHAT IS THE MAX LIMIT OF SUDAFED A PERSON CAN BUY PER MONTH?

TO PURCHASE SUDAFED YOU MUST COMPLETE WHAT STEP(S)?

WHAT IS THE DEFINITION OF ETHICS?

WHAT ARE THE 7 THINGS REQUIRED BY STATE/FEDERAL LAW ON RXS FOR CONTROLLED SUBSTANCES?

THE FEDERAL LAW REGULATING CONTROLLED SUBSTANCES IS :

WHAT IS THE WORKING RATIO OF PHARMACIST TO TECHS?

WHAT IS PHI

HOW LONG DOES DEA FORM 222 HAVE TO BE KEPT ON FILE AT THE PHARMACY?

WHAT IS THE MAX AMOUNT OF SUDAFED A PERSON CAN BUY PER DAY?

WHAT ARE SOME OF THE QUALIFICATIONS FOR PHARM TECH REGISTRATION?

WHAT IS AN OTC?

TO ORDER C2 CONTROLLED SUBSTANCES WHAT FORM HAS TO BE FILLED OUT?

CONTROLLED SUBSTANCES ARE SUBJECT TO STRICTER CONTROLS FROM STATE AND FEDERAL LAWS THAN OTHER DRUGS.

WHAT IS THE FUNCTION OF STATE RX DRUG MONITORING PROGRAMS?

WHO IN THE PHARMACY CAN MAKE THE "OFFER" TO COUNSEL?

WHAT BOOK LISTS BIOLOGICAL PRODUCTS THAT ARE CONSIDERED BIOSIMILAR?

PRESCRIPTION DRUGS ARE ALSO KNOWN AS :

WHAT DOES DEA STAND FOR?

IF THE DOCTOR WANTS THE PATIENT TO GET ONLY THE BRAND NAME THEY WILL WRITE _____ ON THE PRESCRIPTION.

IF STATE AND FEDERAL LAW DIFFER WHAT DO YOU DO?

GENERIC MANUFACTURERS DO NOT NEED TO DEMONSTRATE THAT A DRUG IS BIOQUVALENT TO THE BRAND NAME DRUG.

HOW MANY COPIES ARE THERE OF DEA 222 FORM?

WHAT LAW MADE IN 1996 GOVERNS PATIENT PRIVACY?

WHAT TYPE OF INFORMATION IS ON PACKAGE INSERTS?

HOW MANY REFILLS CAN C2 RXS HAVE?

WHO IS RESPONSIBLE FOR REGULATING THE PRACTICE OF PHARMACY?

HOW MANY TIMES CAN C3 - C5 BE TRANSFERED

SUDAFED (PSEUDOEPHEDRINE) IS ALSO KNOWN AS A?

WHAT ARE THE 5 CLASSES OF CONTROLLED SUBSTANCES?

WHAT IS THE SECOND LETTER OF A PHYSICIANS DEA #?

WHAT DOES BIENNIAL MEAN?

PHARMACY LAWS MAY VARY FROM STATE TO STATE.

WHAT REFERENCE BOOK LISTS GENERIC DRUGS THAT ARE THERAPEUTICALLY EQUIVALENT?

WHAT LAW COVERS PATIENT COUNSELING ESPECIALLY TO MEDICAID PATIENTS?

WHAT SYMBOL WILL APPEAR ON A CONTROLLED SUBSTANCE STOCK BOTTLE?

WHEN A NEW DRUG IS DEVELOPED THE MANUFACTURER MUST COMPLETE A :

AFTER A PATENT EXPIRES AND DRUG COMPANY CAN MAKE THE GENERIC, THE MUST COMPLETE A(N)___ TO SUBMIT TO THE FDA.