Statements (25)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:United_States_federal_law
|
| gptkbp:alsoKnownAs |
Section 353 of Title 21, U.S. Code
|
| gptkbp:appliesTo |
over-the-counter drugs
prescription drugs |
| gptkbp:citation |
gptkb:Drug_Supply_Chain_Security_Act
Prescription Drug Marketing Act |
| gptkbp:containsProvision |
exemptions for investigational drugs
requirements for compounding pharmacies requirements for distribution of drug samples requirements for drug samples requirements for prescription drug labeling requirements for prescription drug marketing requirements for refilling prescriptions requirements for veterinary drugs |
| gptkbp:enforcedBy |
gptkb:Drug_Enforcement_Administration
gptkb:U.S._Food_and_Drug_Administration |
| https://www.w3.org/2000/01/rdf-schema#label |
21 U.S.C. § 353
|
| gptkbp:jurisdiction |
gptkb:United_States
|
| gptkbp:partOf |
gptkb:Title_21_of_the_United_States_Code
|
| gptkbp:regulates |
dispensing of prescription drugs
distribution of prescription drugs exemptions for certain drugs labeling of prescription drugs |
| gptkbp:bfsParent |
gptkb:Title_21_of_the_United_States_Code
|
| gptkbp:bfsLayer |
7
|