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Use of Ozone-Depleting Substances; Removal of Essential-Use Designation (Epinephrine)

other · Food and Drug Administration · Rule · Published 2008-11-19 · Effective 2011-12-31 · 73 FR 69532

Document

Document number
E8-27436
Federal Register citation
73 FR 69532
CFR reference
21 CFR 2
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2008-11-19
Effective date
2011-12-31
HHS docket
Docket No. FDA-2007-N-0314

Abstract

The Food and Drug Administration (FDA), after consultation with the Environmental Protection Agency (EPA), is amending FDA's regulation on the use of ozone-depleting substances (ODSs) in self- pressurized containers to remove the essential-use designation for epinephrine used in oral pressurized metered-dose inhalers (MDIs). The Clean Air Act requires FDA, in consultation with the EPA, to determine whether an FDA-regulated product that releases an ODS is an essential use of the ODS. FDA has concluded that there are no substantial technical barriers to formulating epinephrine as a product that does not release ODSs, and therefore epinephrine would no longer be an essential use of ODSs as of December 31, 2011. Epinephrine MDIs containing an ODS cannot be marketed after this date.

Source

Authoritative
Federal Register document
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