Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:United_States_federal_law
|
| gptkbp:administeredBy |
gptkb:U.S._Food_and_Drug_Administration
|
| gptkbp:appliesTo |
over-the-counter drugs
prescription drugs bulk drug substances finished drug products |
| gptkbp:codifiedIn |
gptkb:21_U.S.C._§_360
|
| gptkbp:dateEnacted |
1972
|
| gptkbp:enables |
FDA to monitor drug safety
FDA to recall drugs if necessary |
| gptkbp:enactedBy |
gptkb:United_States_Congress
|
| gptkbp:established |
National Drug Code (NDC) system
|
| gptkbp:partOf |
gptkb:Federal_Food,_Drug,_and_Cosmetic_Act
|
| gptkbp:purpose |
to provide FDA with a current list of all drugs in commercial distribution
|
| gptkbp:relatedTo |
Drug approval process
Drug labeling Drug registration |
| gptkbp:requires |
drug manufacturers to register with FDA
drug manufacturers to list all commercially marketed drugs with FDA |
| gptkbp:bfsParent |
gptkb:National_Drug_Code_(United_States)
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Drug Listing Act of 1972
|