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Laws

TermDefinition
DEA Form 222 TRANSFER OR ORDER SCHEDULED II SUBSTANCES
DEA FORM 224 TO BE ALLOWED TO DISPENSE CONTROLLLED SUBSTANCE
DEA FORM 106 TO REPORT LOSS OR STOLEN CONTROLLED SUBSTANCES
DEA FORM 41 USE TO DESTROY CONTROLLED SUBSTANCES
DAW 0 NO PRODUCT SELECTION INDICATED
DAW 1 SUBSTITUTION NOT ALLOWED BY PRESCRIBER
DAW 2 SUBSTITUTION ALLOWED (PATIENT REQUESTED)
DAW 3 SUBSTITUTION ALLOWED (RPH SELECTED PRODUCT)
DAW 4 SUBSTTIUTION ALLOWED (GENERIC NOT IN STOCK)
DAW 5 SUBSTITUTION ALLOWED (BRAND DISPENSED AS A GENERIC)
DAW 6 OVERRIDE
DAW 7 SUBSTITUTION NOT ALLOWED (BRAND DRUG MANDATED BY LAW)
DAW 8 SUBSTITUTION ALLOWED (GENERIC DRUG NOT AVAILABLE IN MARKETPLACE)
DAW 9 SUBSTITUTION ALLOWED BY PRESCRIBER BUT PLAN REQUESTS BRAND
NDC FIRST # MANUFACTURER/LABELER CODE
NDC SECOND # PRODUCT CODE/ MEDICATION
NDC THIRD # PACKAGE SIZE
PURE FOOD AND DRUG ACT THE FIRST ESTABLISHED LEGISLATION TO REGULATE DRUGS PASSED IN 1906
CONTROLLED SUBSTANCE ACT THE LEGISLATION INTRODUCED MEASURES FOR THE SAFE ORGANIZATION OF CONTROLLED SUBSTANCES WITH HIGH ABUSE POTENTIAL. PASSED IN 1970
POISON PREVENTION PACKAGING ACT CHILD RESISTANT PACKAGING. PASSED IN 1970
OCCUPATIONAL HEALTH AND SAFETY ACT TO PREVENT WORKPLACE ILLNESS AND INJURY. PASSED IN 1970
ORPHAN DRUG ACT DRUGS USED TO TREAT RARE DISEASES. PASSED IN 1983
OMNIBUS BUDGET RECONCILIATION ACT (OBRA 90) OFFER COUNSELING TO PATIENTS. PASSED IN 1990
DRUG LISITING ACT ACCURATE INDENTIFICATION OF MEDICINES. EACH MEDICATION WILL HAVE IT'S OWN NDC. PASSED IN 1972
FOOD, DRUG, AND COSMETIC ACT TIGHTENED CONTROLS OVER DRUGS AND FOOD AND ENHANCED GOVERNMENT ABILITY TO ENFORE THE LAW. PASSED IN 1938
KEFAUVER-HARRIS AMENDMENT GURANTEED THE SAFETY, PURITY, AND EFFICACY OF BOTH PRESCRIPTION AND NON PRESCRIPTION MEDICATION. PASSED IN 1962
DURHAM-HUMPHREY AMENDMENT CATEGORZIED LEGEND AND OTC DRUGS. PASSED IN 1951
HEALTH INSURANCE PROTABILITY AND ACCOUNTABILITY ACT PROTECTS PATIENT INFORMATION AND LIMITS HOW HEALTHCARE PROVIDERS DISCLOSE INFORMATION
COMEBAT METHAMPHETAMINE EPIDEMIC ACT LIMITS PSEUDOEPHEDRINE AND EPHEDRINE SALES TO 3.6 GRAMS PER DAY/9 GRAMS PER MONTH. PASSED IN 2005
FEDERAL DRUG ADMINISTRATION (FDA) SUPERVISES DEVELOPMENT, TESTING, PURITY, SAFETY, AND EFFECTIVENESS OF RX AND OTC MEDICATIONS. PASSED IN 1906
THE JOINT COMMISSION (TJC) ACCREDITS AND CERTIFIES HEALTCARE ORGANIZATIONS
DRUG SUPPLY CHAIN SECURITY ACT (DSCSA) REQUIRES THE TRACKING AND TRACING OF PRESCRIPTION DRUGS IN THE US TO PREVENT CONTERFIET OR UNSAFE PRODUCTS. PASSED IN 2013
MEDICATION RECALL CLASS 1 STRONG CHANCE OF SERIOUS ADVERSE EFFECTS OR DEATH
MEDICATION RECALL CLASS 2 TEMPORARY (BUT REVERSIBLE) CHANCE OF ADVERSE EFFECT OR LITTLE CHANCE OF SERIOUS ADVERSE EFFECT
MEDTICATION RECALL CLASS 3 NOT LIKELY TO CAUSE ADVERSE EFFECTS
SCHEDULE 2 CONTROLLED SUBSTANCE NO REFILLS HIGH ABUSE
SCHEDULE 3-5 CONTROLLED SUBSTANCE 5 REFILLS MODERATE TO LIMITED ABUSE
Created by: PT Instructor
 

 



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