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| HHS/FDA | RIN: 0910-AC18 | Publication ID: Spring 2002 |
| Title: Aluminum in Large- and Small-Volume Parenterals Used in Total Parenteral Nutrition | |
| Abstract: The proposed rule would revise 21 CFR 323(c) to permit small-volume parenterals and pharmacy bulk packages that contain no more than 25 ug/L of aluminum to state "contains no more than 25ug/L" rather than the exact amount of aluminum. | |
| Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
| RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Proposed Rule Stage |
| Major: No | Unfunded Mandates: No |
| CFR Citation: 21 CFR 201.323(c) | |
| Legal Authority: 21 USC 321(n) 21 USC 352 21 USC 355 21 USC 371(a) 21 CFR 201.51 21 CFR 201.100 21 CFR 314.125 | |
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Legal Deadline:
None |
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Timetable:
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| Regulatory Flexibility Analysis Required: Undetermined | Government Levels Affected: None |
| Small Entities Affected: No | Federalism: No |
| Included in the Regulatory Plan: No | |
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Agency Contact: Christine F. Rogers Regulatory Counsel Department of Health and Human Services Food and Drug Administration Suite 3059 (HFD-7), Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, Bldg. 51, Room 6316, Silver Spring, MD 20993-0002 Phone:301 796-3601 Fax:301 847-8440 Email: christine.rogers@fda.hhs.gov |
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