Abstract
In the case of an FDA shortage of drug X, an injectable medication, the safer route to supply the drug to hospital systems would be through a 503B outsourcing facility. Unlike 503A pharmacies, 503B outsourcing facilities are permitted to compound medications in larger batches and are held to stricter FDA oversight. They must comply with current good manufacturing practices (cGMP), which help ensure the quality of medications intended for broader distribution during drug shortages in hospital systems.
| Original language | English |
|---|---|
| Pages (from-to) | 120-129 |
| Number of pages | 10 |
| Journal | International Journal of Pharmaceutical Compounding |
| Volume | 30 |
| Issue number | 2 |
| State | Published - 2026 |
| Externally published | Yes |
Keywords
- United States
- United States Food and Drug Administration
- Drug Compounding/ethics
- Humans
- Outsourced Services/ethics
- Pharmaceutical Preparations/supply & distribution
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