Abstract
Abuse-deterrent formulations are one strategy for mitigating the epidemic of prescription opioid abuse. Regulatory guidance documents describe the requirements for developing abuse-deterrent formulations of novel drugs and formulations; however, they do not address "abuse-deterrence equivalence" for generic formulations. As generics may be produced with different excipients and formulations compared to reference drugs, differences in their properties may impact their abuse-deterrent features. Currently, it is unclear what specific studies are needed to support generic abuse-deterrence claims. This commentary outlines several recommendations on the in vitro and in vivo testing required, including the conditions for conducting a human abuse potential study.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 96-100 |
| Number of pages | 5 |
| Journal | Journal of Opioid Management |
| Volume | 12 |
| Issue number | 2 |
| DOIs | |
| State | Published - May 1 2016 |
| Externally published | Yes |
ASJC Scopus subject areas
- General Medicine
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