21 CFR 316.4 - Address for submissions.
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All correspondence and requests for FDA action under the provisions of this rule should be addressed as follows: Office of Orphan Products Development, Food and Drug Administration, Bldg. 32, Rm. 5271, 10903 New Hampshire Ave., Silver Spring, MD 20993.
[78 FR 35133, June 12, 2013]
Title 21 published on 2014-04-01
no entries appear in the Federal Register after this date.