No prescription drug or drug composed wholly or partly of insulin that was manufactured in a State and exported from the United States may be reimported by anyone other than its manufacturer, except that FDA may grant permission to a person other than the manufacturer to reimport a prescription drug or insulin-containing drug if it determines that such reimportation is required for emergency medical care.
21 CFR Part 203 · Prescription Drug Marketing
§ 203.10 Restrictions on reimportation
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Amendment history
Federal Register documents that created or amended this section.
- 64 FR 67756 3 Dec 1999