Publication | Closed Access
Abuses of FDA Regulatory Procedures — The Case of Suboxone
11
Citations
3
References
2020
Year
Drug PolicyBrand-name Buprenorphine ProductsRegulatory Safety ScienceHarm ReductionManagementToxicologyRegulatory ConsiderationDrug SafetyFda Regulatory ProceduresHealth PolicyPharmacoeconomicsPharmacologyAdvertisingMarketingSubstance AbuseGeneric CompetitorsRegulatory ApprovalPrescription-drug MarketsMedicineRegulationPrescription Drugs
The manufacturer of brand-name buprenorphine products exploited various FDA regulatory procedures to impede market entry of generic competitors and to maintain high prices. This case provides an example of the kinds of abuses that are common in prescription-drug markets.
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